No renderable structure data available
FC1C=CC2CC(NC=2C=1)=OChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 6-Fluoro-2-oxindole |
|---|---|
| IUPAC Name | — |
| CAS Number | 56341-39-0 |
| Database ID | 3731013 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
6-Fluoro-2-oxindole (CAS 56341-39-0) 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 3731013
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-8f727760975f427787ab54aad7e4044fConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-aabad8f1cf874f71b60d4d849750f10eConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-dfe3d1aac9db45389ee7d8f85d1877b8Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-779fb6c052fe4eea9f7b895c78cf43c2Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-65b02af726d64718b7667dfbfbe4c5fcConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-c395bfbaf1b74867be7af9051621acfaConditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: To a solution of 6-fluorooxindole (3 g, 20 mmol) in THF (50 mL) at 0° C., was added 40 mL of 1M LHMDS in THF. The reaction mixture was stirred at 0° C. for 15 minutes. A solution of 4-bromo-5, 5-dimethyl-5H-furan-2-one (5) (1.91 g, 10 mmol) in 5 mL of THF was added to the above reaction mixture. The reaction was stirred at 0° C. for further 30 minutes and then at room temperature for 2.5 hrs. To the reaction, 80 mL of 2M HCl was added. The resulting mixture was stirred at 50-55° C. for one hour, cooled down to room temperature, poured to 1000 mL of water and was stirred at room temperature for one hour. The precipitates formed were collected and washed with water, dried in vacuum to give the title compound as a yellow solid product (2.4 g, yield: 74%). The reaction was stirred at 0° C. for further 30 minutes at room temperature for 2.5 hrs was added The resulting mixture was stirred at 50-55° C. for one hour cooled down to room temperature was stirred at room temperature for one hour The precipitates formed were collected washed with water dried in vacuum
Source ID: ord-83ac01274e974ca5a0079bccd05b3499Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: To a 0° C. stirred solution of 6-fluorooxindole (370 mg, 2.45 mmol) in anhydrous THF (10 mL) was added 1M LiHMDS/THF solution (4.9 mL, 4.9 mmol). The mixture was stirred at 0° C. for 10 minutes. 4-Bromo-5H-furan-2-one (200 mg, 1.23) was added as a solution in 2 mL of THF. The resulting mixture was stirred at 0° C. for 30 minutes, then at room temperature for 1 hour and quenched with 10 mL of 2M HCl. Methanol (5 mL) was added and the mixture was stirred at 50° C. for 0.5 hour. The mixture was poured into 150 mL of water and then stirred for 30 minutes. The precipitates were filtered, washed with water, and dried in vacuum to give 3-(4-bromo-5H-furan-2-ylidene)-6-fluoro-1,3-dihydro-indol-2-one as a yellow solid. Yield: 228 mg, 63%. The resulting mixture was stirred at 0° C. for 30 minutes at room temperature for 1 hour quenched with 10 mL of 2M HCl Methanol (5 mL) was added the mixture was stirred at 50° C. for 0.5 hour The mixture was poured into 150 mL of water stirred for 30 minutes The precipitates were filtered washed with water dried in vacuum
Source ID: ord-ea051f6b120a48f1baf1202b2458ae29Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: To a stirred solution of 6-fluorooxindole (2.6 g, 17.5 mmol) in anhydrous THF (30 mL) under nitrogen was added 1.0 M LiHMDS/THF solution (35 mL, 35 mmol). The mixture was stirred at room temperature for 10 minutes. Methyl tetronate (1.0 g, 8.8 mmol) was added as one portion. After stirring at room temperature for 1 hour, the reaction was cooled to 0° C., and quenched with 2M HCl until pH=3. The mixture was stirred at room temperature for 2 more hours, and poured into 250 mL of water. The resulting precipitates were filtered, rinsed with water and dried in vacuum to give 6-fluoro-3-(4-methoxy-5H-furan-2-ylidene)-1,3-dihydro-indol-2-one as off-white solid. Yield: 840 mg, 38%. After stirring at room temperature for 1 hour the reaction was cooled to 0° C. quenched with 2M HCl until pH=3 The mixture was stirred at room temperature for 2 more hours poured into 250 mL of water The resulting precipitates were filtered rinsed with water dried in vacuum
Source ID: ord-b1efd9c2b7b045e18a00bbc540fa478fConditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: To a solution of 6-fluorooxindole (3 g, 20 mmol) in THF (50 mL) at 0° C., was added 40 mL of 1M LHMDS in THF. The reaction mixture was stirred at 0° C. for 15 minutes. A solution of 4-bromo-5,5-dimethyl-5H-furan-2-one (5) (1.91 g, 10 mmol) in 5 mL of THF was added to the above reaction mixture. The reaction was stirred at 0° C. for further 30 minutes and then at room temperature for 2.5 hrs. To the reaction, 80 mL of 2M HCl was added. The resulting mixture was stirred at 50-55° C. for one hour, cooled down to room temperature, poured to 1000 mL of water and was stirred at room temperature for one hour. The precipitates formed were collected and washed with water, dried in vacuum to give the title compound as a yellow solid product (2.4 g, yield: 74%). The reaction was stirred at 0° C. for further 30 minutes at room temperature for 2.5 hrs was added The resulting mixture was stirred at 50-55° C. for one hour cooled down to room temperature was stirred at room temperature for one hour The precipitates formed were collected washed with water dried in vacuum
Source ID: ord-cd99692ef85541fcb4a16ff75769c566Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: To a 0° C. stirred solution of 6-fluorooxindole (370 mg, 2.45 mmol) in anhydrous THF (10 mL) was added 1M LiHMDS/THF solution (4.9 mL, 4.9 mmol). The mixture was stirred at 0° C. for 10 minutes. 4-Bromo-5H-furan-2-one (200 mg, 1.23) was added as a solution in 2 mL of THF. The resulting mixture was stirred at 0° C. for 30 minutes, then at room temperature for 1 hour and quenched with 10 mL of 2M HCl. Methanol (5 mL) was added and the mixture was stirred at 50° C. for 0.5 hour. The mixture was poured into 150 mL of water and then stirred for 30 minutes. The precipitates were filtered, washed with water, and dried in vacuum to give 3-(4-bromo-5H-furan-2-ylidene)-6-fluoro-1,3-dihydro-indol-2-one as a yellow solid. Yield: 228 mg, 63%. The resulting mixture was stirred at 0° C. for 30 minutes at room temperature for 1 hour quenched with 10 mL of 2M HCl Methanol (5 mL) was added the mixture was stirred at 50° C. for 0.5 hour The mixture was poured into 150 mL of water stirred for 30 minutes The precipitates were filtered washed with water dried in vacuum
Source ID: ord-3bb8a73c97074de1b49c3cccdef658fbConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: To a stirred solution of 6-fluorooxindole (2.6 g, 17.5 mmol) in anhydrous THF (30 mL) under nitrogen was added 1.0M LiHMDS/THF solution (35 mL, 35 mmol). The mixture was stirred at room temperature for 10 minutes. Methyl tetronate (1.0 g, 8.8 mmol) was added as one portion. After stirring at room temperature for 1 hour, the reaction was cooled to 0° C., and quenched with 2M HCl until pH=3. The mixture was stirred at room temperature for 2 more hours, and poured into 250 mL of water. The resulting precipitates were filtered, rinsed with water and dried in vacuum to give 6-fluoro-3-(4-methoxy-5H-furan-2-ylidene)-1,3-dihydro-indol-2-one as off-white solid. Yield: 840 mg, 38%. After stirring at room temperature for 1 hour the reaction was cooled to 0° C. quenched with 2M HCl until pH=3 The mixture was stirred at room temperature for 2 more hours poured into 250 mL of water The resulting precipitates were filtered rinsed with water dried in vacuum
Source ID: ord-63bc797482c34a3ca866297acc8a62d6PubChem References
These sources are listed in the compound's public database record.
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