No renderable structure data available
C1=CC(=C(C=C1Cl)O)C(=O)NChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 4-chloro-2-hydroxybenzamide |
|---|---|
| IUPAC Name | — |
| CAS Number | 37893-37-1 |
| Database ID | 13726281 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
4-chloro-2-hydroxybenzamide (CAS 37893-37-1) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 13726281
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
12 reactions · 12 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-37809a630b2e47398d7d0a88b1aa9825Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A 22 L, five neck, round bottom flask was equipped with an overhead stirrer, reflux condenser, addition funnel, thermocouple temperature read out, and a heating mantle. The reactor was purged with nitrogen. Acetonitrile (4700 mL) and 4-chloro-2-hydroxybenzamide (1782 g, 10.4 mol) were charged to the reaction flask and the stirring was started. Pyridine (1133 mL, 14.0 mol) was charged to the reactor. The resulting reaction slurry was cooled to less than 10° C. with an ice bath. Ethyl chloroformate (1091 mL, 1237 g, 11.4 mol) was placed in the addition funnel and charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition. The temperature of the reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours. Liquid chromatographic analysis of the reaction mixture indicated that the reaction was only 80% complete. Approximately half of the solvent was removed by atmospheric distillation. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Additional pyridine (215 mL, 2.65 mol) was added to the reaction mixture. Ethyl chloroformate (235 g, 2.17 mol) was added slowly via an addition funnel to the cold reaction mixture. The reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours, after which time liquid chromatographic analysis indicated that the reaction was complete. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Water (1600 mL) was added slowly via an addition funnel and the resulting slurry held at <10° C. for 90 minutes. The solid product was collected by vacuum filtration through a large sintered glass funnel. The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours to give 1914 g of 7-chloro-2H-1,3-benzoxazine-2,4(3H)-dione as a tan solid. The yield was 83%. A 22 L, five neck, round bottom flask was equipped with an overhead stirrer reflux condenser, addition funnel The reactor was purged with nitrogen The resulting reaction slurry was cooled to less than 10° C. with an ice bath charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition The ice bath was removed The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours Approximately half of the solvent was removed by atmospheric distillation The reaction mixture was cooled first to ambient temperature to <10° C. The reaction mixture was held between 10 and 15° C. for 30 minutes The ice bath was removed the reaction mixture was warmed to ambient temperature The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours The reaction mixture was cooled first to ambient temperature to <10° C. Water (1600 mL) was added slowly via an addition funnel the resulting slurry held at <10° C. for 90 minutes The solid product was collected by vacuum filtration through a large sintered glass funnel The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours
Source ID: ord-be9a13514b124582b4e988df906f7c96Conditions: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: To a solution of 4-chloro-2-hydroxybenzamide (0.608 g, 3.54 mmol) in acetonitrile (50 ml) was added dried K2CO3 (1.71 g, 12.40 mmol) followed by benzyl bromide (0.63 ml, 5.32 mmol) and the resulting reaction mixture was refluxed at 80° C. for 16 h. After the completion of the reaction (TLC monitoring), water was added followed by extraction with EtOAc (3×100 ml). The combined organics was dried over anhydrous Na2SO4, filtered and concentrated. The residue was washed repeatedly with hexane to get rid of the excess of benzyl bromide resulting the desired product (0.75 g, 81%). the resulting reaction mixture was added followed by extraction with EtOAc (3×100 ml) The combined organics was dried over anhydrous Na2SO4 filtered concentrated The residue was washed repeatedly with hexane
Source ID: ord-7f482b0b6c1e495baffb4737c430c5a2Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 4-chloro-2-methoxybenzamide (0.74 g, 3.99 mmol) in dichloromethane (50 ml) was cooled to −78° C. followed by addition of BBr3 (1.15 ml, 11.96 mmol) under nitrogen atmosphere. The reaction mixture was allowed to stir at room temperature for 2 h. After the completion of reaction (TLC monitoring), the solution was cooled to 0° C. and quenched with water. The resulting solution was basified by aqueous NaHCO3 and extracted with EtOAc (3×100 ml). The combined organics was dried over anhydrous Na2SO4, filtered and concentrated to get the desired product (0.608 g, 89%). MS: 172.33 (M+H)+. After the completion of reaction (TLC monitoring) the solution was cooled to 0° C. quenched with water extracted with EtOAc (3×100 ml) The combined organics was dried over anhydrous Na2SO4 filtered concentrated
Source ID: ord-c3198b94586846e1b2b985583f7ddd94Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 4-chloro-2-methoxybenzamide (0.74 g, 3.99 mmol) in dichloromethane (50 ml) was cooled to −78° C. followed by addition of BBr3 (1.15 ml, 11.96 mmol) under nitrogen atmosphere. The reaction mixture was allowed to stir at room temperature for 2 h. After the completion of reaction (TLC monitoring), the solution was cooled to 0° C. and quenched with water. The resulting solution was basified by aqueous NaHCO3 and extracted with EtOAc (3×100 ml). The combined organics was dried over anhydrous Na2SO4, filtered and concentrated to get the desired product (0.608 g, 89%). MS: 172.33 (M+H)+. After the completion of reaction (TLC monitoring) the solution was cooled to 0° C. quenched with water extracted with EtOAc (3×100 ml) The combined organics was dried over anhydrous Na2SO4 filtered concentrated
Source ID: ord-c3198b94586846e1b2b985583f7ddd94Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A 22 L, five neck, round bottom flask was equipped with an overhead stirrer, reflux condenser, addition funnel, thermocouple temperature read out, and a heating mantle. The reactor was purged with nitrogen. Acetonitrile (4700 mL) and 4-chloro-2-hydroxybenzamide (1782 g, 10.4 mol) were charged to the reaction flask and the stirring was started. Pyridine (1133 mL, 14.0 mol) was charged to the reactor. The resulting reaction slurry was cooled to less than 10° C. with an ice bath. Ethyl chloroformate (1091 mL, 1237 g, 11.4 mol) was placed in the addition funnel and charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition. The temperature of the reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours. Liquid chromatographic analysis of the reaction mixture indicated that the reaction was only 80% complete. Approximately half of the solvent was removed by atmospheric distillation. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Additional pyridine (215 mL, 2.65 mol) was added to the reaction mixture. Ethyl chloroformate (235 g, 2.17 mol) was added slowly via an addition funnel to the cold reaction mixture. The reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours, after which time liquid chromatographic analysis indicated that the reaction was complete. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Water (1600 mL) was added slowly via an addition funnel and the resulting slurry held at <10° C. for 90 minutes. The solid product was collected by vacuum filtration through a large sintered glass funnel. The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours to give 1914 g of 7-chloro-2H-1,3-benzoxazine-2,4(3H)-dione as a tan solid. The yield was 83%. A 22 L, five neck, round bottom flask was equipped with an overhead stirrer reflux condenser, addition funnel The reactor was purged with nitrogen The resulting reaction slurry was cooled to less than 10° C. with an ice bath charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition The ice bath was removed The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours Approximately half of the solvent was removed by atmospheric distillation The reaction mixture was cooled first to ambient temperature to <10° C. The reaction mixture was held between 10 and 15° C. for 30 minutes The ice bath was removed the reaction mixture was warmed to ambient temperature The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours The reaction mixture was cooled first to ambient temperature to <10° C. Water (1600 mL) was added slowly via an addition funnel the resulting slurry held at <10° C. for 90 minutes The solid product was collected by vacuum filtration through a large sintered glass funnel The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours
Source ID: ord-50418000df3c4e5ab749dc6067e26e8bConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-37809a630b2e47398d7d0a88b1aa9825Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A 22 L, five neck, round bottom flask was equipped with an overhead stirrer, reflux condenser, addition funnel, thermocouple temperature read out, and a heating mantle. The reactor was purged with nitrogen. Acetonitrile (4700 mL) and 4-chloro-2-hydroxybenzamide (1782 g, 10.4 mol) were charged to the reaction flask and the stirring was started. Pyridine (1133 mL, 14.0 mol) was charged to the reactor. The resulting reaction slurry was cooled to less than 10° C. with an ice bath. Ethyl chloroformate (1091 mL, 1237 g, 11.4 mol) was placed in the addition funnel and charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition. The temperature of the reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours. Liquid chromatographic analysis of the reaction mixture indicated that the reaction was only 80% complete. Approximately half of the solvent was removed by atmospheric distillation. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Additional pyridine (215 mL, 2.65 mol) was added to the reaction mixture. Ethyl chloroformate (235 g, 2.17 mol) was added slowly via an addition funnel to the cold reaction mixture. The reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours, after which time liquid chromatographic analysis indicated that the reaction was complete. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Water (1600 mL) was added slowly via an addition funnel and the resulting slurry held at <10° C. for 90 minutes. The solid product was collected by vacuum filtration through a large sintered glass funnel. The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours to give 1914 g of 7-chloro-2H-1,3-benzoxazine-2,4(3H)-dione as a tan solid. The yield was 83%. A 22 L, five neck, round bottom flask was equipped with an overhead stirrer reflux condenser, addition funnel The reactor was purged with nitrogen The resulting reaction slurry was cooled to less than 10° C. with an ice bath charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition The ice bath was removed The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours Approximately half of the solvent was removed by atmospheric distillation The reaction mixture was cooled first to ambient temperature to <10° C. The reaction mixture was held between 10 and 15° C. for 30 minutes The ice bath was removed the reaction mixture was warmed to ambient temperature The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours The reaction mixture was cooled first to ambient temperature to <10° C. Water (1600 mL) was added slowly via an addition funnel the resulting slurry held at <10° C. for 90 minutes The solid product was collected by vacuum filtration through a large sintered glass funnel The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours
Source ID: ord-50418000df3c4e5ab749dc6067e26e8bConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A 22 L, five neck, round bottom flask was equipped with an overhead stirrer, reflux condenser, addition funnel, thermocouple temperature read out, and a heating mantle. The reactor was purged with nitrogen. Acetonitrile (4700 mL) and 4-chloro-2-hydroxybenzamide (1782 g, 10.4 mol) were charged to the reaction flask and the stirring was started. Pyridine (1133 mL, 14.0 mol) was charged to the reactor. The resulting reaction slurry was cooled to less than 10° C. with an ice bath. Ethyl chloroformate (1091 mL, 1237 g, 11.4 mol) was placed in the addition funnel and charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition. The temperature of the reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours Liquid chromatographic analysis of the reaction mixture indicated that the reaction was only 80% complete. Approximately half of the solvent was removed by atmospheric distillation. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Additional pyridine (215 mL, 2.65 mol) was added to the reaction mixture. Ethyl chloroformate (235 g, 2.17 mol) was added slowly via an addition funnel to the cold reaction mixture. The reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours, after which time liquid chromatographic analysis indicated that the reaction was complete. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Water (1600 mL) was added slowly via an addition funnel and the resulting slurry held at <10° C. for 90 minutes. The solid product was collected by vacuum filtration through a large sintered glass funnel. The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours to give 1914 g of 7-chloro-2H-1,3-benzoxazine-2,4 (3H)-dione as a tan solid. The yield was 83%. A 22 L, five neck, round bottom flask was equipped with an overhead stirrer reflux condenser, addition funnel The reactor was purged with nitrogen The resulting reaction slurry was cooled to less than 10° C. with an ice bath charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition The ice bath was removed The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours Approximately half of the solvent was removed by atmospheric distillation The reaction mixture was cooled first to ambient temperature to <10° C. The reaction mixture was held between 10 and 15° C. for 30 minutes The ice bath was removed the reaction mixture was warmed to ambient temperature The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours The reaction mixture was cooled first to ambient temperature to <10° C. Water (1600 mL) was added slowly via an addition funnel the resulting slurry held at <10° C. for 90 minutes The solid product was collected by vacuum filtration through a large sintered glass funnel The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours
Source ID: ord-3dc52bcfd8a34943a7771b270c57614cConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A 22 L, five neck, round bottom flask was equipped with an overhead stirrer, reflux condenser, addition funnel, thermocouple temperature read out, and a heating mantle. The reactor was purged with nitrogen. Acetonitrile (4700 mL) and 4-chloro-2-hydroxybenzamide (1782 g, 10.4 mol) were charged to the reaction flask and the stirring was started. Pyridine (1133 mL, 14.0 mol) was charged to the reactor. The resulting reaction slurry was cooled to less than 10° C. with an ice bath. Ethyl chloroformate (1091 mL, 1237 g, 11.4 mol) was placed in the addition funnel and charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition. The temperature of the reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours Liquid chromatographic analysis of the reaction mixture indicated that the reaction was only 80% complete. Approximately half of the solvent was removed by atmospheric distillation. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Additional pyridine (215 mL, 2.65 mol) was added to the reaction mixture. Ethyl chloroformate (235 g, 2.17 mol) was added slowly via an addition funnel to the cold reaction mixture. The reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours, after which time liquid chromatographic analysis indicated that the reaction was complete. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Water (1600 mL) was added slowly via an addition funnel and the resulting slurry held at <10° C. for 90 minutes. The solid product was collected by vacuum filtration through a large sintered glass funnel. The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours to give 1914 g of 7-chloro-2H-1,3-benzoxazine-2,4 (3H)-dione as a tan solid. The yield was 83%. A 22 L, five neck, round bottom flask was equipped with an overhead stirrer reflux condenser, addition funnel The reactor was purged with nitrogen The resulting reaction slurry was cooled to less than 10° C. with an ice bath charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition The ice bath was removed The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours Approximately half of the solvent was removed by atmospheric distillation The reaction mixture was cooled first to ambient temperature to <10° C. The reaction mixture was held between 10 and 15° C. for 30 minutes The ice bath was removed the reaction mixture was warmed to ambient temperature The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours The reaction mixture was cooled first to ambient temperature to <10° C. Water (1600 mL) was added slowly via an addition funnel the resulting slurry held at <10° C. for 90 minutes The solid product was collected by vacuum filtration through a large sintered glass funnel The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours
Source ID: ord-3dc52bcfd8a34943a7771b270c57614cConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A 22L, five neck, round bottom flask was equipped with an overhead stirrer, reflux condenser, addition funnel, thermocouple temperature read out, and a heating mantle. The reactor was purged with nitrogen. Acetonitrile (4700 mL) and 4-chloro-2-hydroxybenzamide (1782 g, 10.4 mol) were charged to the reaction flask and the stirring was started. Pyridine (1133 mL, 14.0 mol) was charged to the reactor. The resulting reaction slurry was cooled to less than 10° C. with an ice bath. Ethyl chloroformate (1091 mL, 1237 g, 11.4 mol) was placed in the addition funnel and charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition. The temperature of the reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours. Liquid chromatographic analysis of the reaction mixture indicated that the reaction was only 80% complete. Approximately half of the solvent was removed by atmospheric distillation. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Additional pyridine (215 mL, 2.65 mol) was added to the reaction mixture. Ethyl chloroformate (235 g, 2.17 mol) was added slowly via an addition funnel to the cold reaction mixture. The reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours, after which time liquid chromatographic analysis indicated that the reaction was complete. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Water (1600 mL) was added slowly via an addition funnel and the resulting slurry held at <10° C. for 90 minutes. The solid product was collected by vacuum filtration through a large sintered glass funnel. The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours to give 1914 g of 7-chloro-2H-1,3-benzoxazine-2,4(3H)-dione as a tan solid. The yield was 83%. reflux condenser, addition funnel The reactor was purged with nitrogen The resulting reaction slurry was cooled to less than 10° C. with an ice bath charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition The ice bath was removed The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours Approximately half of the solvent was removed by atmospheric distillation The reaction mixture was cooled first to ambient temperature to <10° C. The reaction mixture was held between 10 and 15° C. for 30 minutes The ice bath was removed the reaction mixture was warmed to ambient temperature The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours The reaction mixture was cooled first to ambient temperature to <10° C. Water (1600 mL) was added slowly via an addition funnel the resulting slurry held at <10° C. for 90 minutes The solid product was collected by vacuum filtration through a large sintered glass funnel The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours
Source ID: ord-0159875e3b87425c976a82c18f22ae51Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A 22 L, five neck, round bottom flask was equipped with an overhead stirrer, reflux condenser, addition funnel, thermocouple temperature read out, and a heating mantle. The reactor was purged with nitrogen. Acetonitrile (4700 mL) and 4-chloro-2-hydroxybenzamide (1782 g, 10.4 mol) were charged to the reaction flask and the stirring was started. Pyridine (1133 mL, 14.0 mol) was charged to the reactor. The resulting reaction slurry was cooled to less than 10° C. with an ice bath. Ethyl chloroformate (1091 mL, 1237 g, 11.4 mol) was placed in the addition funnel and charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition. The temperature of the reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours. Liquid chromatographic analysis of the reaction mixture indicated that the reaction was only 80% complete. Approximately half of the solvent was removed by atmospheric distillation. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Additional pyridine (215 mL, 2.65 mol) was added to the reaction mixture. Ethyl chloroformate (235 g, 2.17 mol) was added slowly via an addition funnel to the cold reaction mixture. The reaction mixture was held between 10 and 15° C. for 30 minutes after the ethyl chloroformate addition was complete. The ice bath was removed, and the reaction mixture was warmed to ambient temperature. The reaction mixture was then slowly heated to reflux and held at that temperature for 18 hours, after which time liquid chromatographic analysis indicated that the reaction was complete. The reaction mixture was cooled first to ambient temperature and then to <10° C. with an ice bath. Water (1600 mL) was added slowly via an addition funnel and the resulting slurry held at <10° C. for 90 minutes. The solid product was collected by vacuum filtration through a large sintered glass funnel. The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours to give 1914 g of 7-chloro-2H-1,3-benzoxazine-2,4(3H)-dione as a tan solid. The yield was 83%. A 22 L, five neck, round bottom flask was equipped with an overhead stirrer reflux condenser, addition funnel The reactor was purged with nitrogen The resulting reaction slurry was cooled to less than 10° C. with an ice bath charged slowly to the stirred reaction mixture such that the temperature of the reaction mixture did not exceed 15° C. during the addition The ice bath was removed The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours Approximately half of the solvent was removed by atmospheric distillation The reaction mixture was cooled first to ambient temperature to <10° C. The reaction mixture was held between 10 and 15° C. for 30 minutes The ice bath was removed the reaction mixture was warmed to ambient temperature The reaction mixture was then slowly heated to reflux held at that temperature for 18 hours The reaction mixture was cooled first to ambient temperature to <10° C. Water (1600 mL) was added slowly via an addition funnel the resulting slurry held at <10° C. for 90 minutes The solid product was collected by vacuum filtration through a large sintered glass funnel The product filter cake was washed with deionized water and vacuum dried at 50° C. for 18 hours
Source ID: ord-69b103af57b6427fa36f1f72d55b9415PubChem References
These sources are listed in the compound's public database record.
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