No renderable structure data available
COC(=O)C1=CC=CC=C1CNChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | methyl 2-(aminomethyl)benzoate |
|---|---|
| IUPAC Name | — |
| CAS Number | 61088-45-7 |
| Database ID | 2760944 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
methyl 2-(aminomethyl)benzoate (CAS 61088-45-7) 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 2760944
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
8 reactions · 8 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-ab53043f85bf4acc8d31e814fbd29970Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Commercially available amino methylbenzoic acid methyl ester (manufactured by Tokyo Kasei Kogyo Co., Ltd.) (278 mg) was dissolved in methanol (9 ml). Then, the solution was added with 1-methyl-2-imidazole carboxaldehyde (manufactured by Aldrich Corporation) (407 mg) and sodium cyanoborohydride (317 mg), and then adjusted to about pH 5 with acetic acid, followed by stirring at room temperature for 3 days. After completion of the reaction, the solvent was distilled off and the residue was then dissolved in chloroform, followed by washing with a 1 mol/l sodium hydroxide solution. The solution was dried with anhydrous sodium sulfate, and the solvent was distilled off. Subsequently, the residue was dissolved in methanol (6.0 ml) and then added with 1 mol/l sodium hydroxide, followed by stirring at room temperature for 6 hours. After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added and the solvent was distilled off. After that, ethanol was added to remove insoluble matter, the solvent was distilled off, and the residue was then dried, thereby obtaining the subject compound (519 mg) as a pale-yellow foamy substance. After completion of the reaction the solvent was distilled off the residue was then dissolved in chloroform by washing with a 1 mol/l sodium hydroxide solution The solution was dried with anhydrous sodium sulfate the solvent was distilled off Subsequently, the residue was dissolved in methanol (6.0 ml) added with 1 mol/l sodium hydroxide by stirring at room temperature for 6 hours After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added the solvent was distilled off After that, ethanol was added to remove insoluble matter the solvent was distilled off the residue was then dried
Source ID: ord-7e25fbcd556647af89095f19b40122f2Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Commercially available amino methylbenzoic acid methyl ester (manufactured by Tokyo Kasei Kogyo Co., Ltd.) (278 mg) was dissolved in methanol (9 ml). Then, the solution was added with 1-methyl-2-imidazole carboxaldehyde (manufactured by Aldrich Corporation) (407 mg) and sodium cyanoborohydride (317 mg), and then adjusted to about pH 5 with acetic acid, followed by stirring at room temperature for 3 days. After completion of the reaction, the solvent was distilled off and the residue was then dissolved in chloroform, followed by washing with a 1 mol/l sodium hydroxide solution. The solution was dried with anhydrous sodium sulfate, and the solvent was distilled off. Subsequently, the residue was dissolved in methanol (6.0 ml) and then added with 1 mol/l sodium hydroxide, followed by stirring at room temperature for 6 hours. After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added and the solvent was distilled off. After that, ethanol was added to remove insoluble matter, the solvent was distilled off, and the residue was then dried, thereby obtaining the subject compound (519 mg) as a pale-yellow foamy substance. After completion of the reaction the solvent was distilled off the residue was then dissolved in chloroform by washing with a 1 mol/l sodium hydroxide solution The solution was dried with anhydrous sodium sulfate the solvent was distilled off Subsequently, the residue was dissolved in methanol (6.0 ml) added with 1 mol/l sodium hydroxide by stirring at room temperature for 6 hours After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added the solvent was distilled off After that, ethanol was added to remove insoluble matter the solvent was distilled off the residue was then dried
Source ID: ord-7e25fbcd556647af89095f19b40122f2Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Commercially available amino methylbenzoic acid methyl ester (manufactured by Tokyo Kasei Kogyo Co., Ltd.) (278 mg) was dissolved in methanol (9 ml). Then, the solution was added with 1-methyl-2-imidazole carboxaldehyde (manufactured by Aldrich Corporation) (407 mg) and sodium cyanoborohydride (317 mg), and then adjusted to about pH 5 with acetic acid, followed by stirring at room temperature for 3 days. After completion of the reaction, the solvent was distilled off and the residue was then dissolved in chloroform, followed by washing with a 1 mol/l sodium hydroxide solution. The solution was dried with anhydrous sodium sulfate, and the solvent was distilled off. Subsequently, the residue was dissolved in methanol (6.0 ml) and then added with 1 mol/l sodium hydroxide, followed by stirring at room temperature for 6 hours. After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added and the solvent was distilled off. After that, ethanol was added to remove insoluble matter, the solvent was distilled off, and the residue was then dried, thereby obtaining the subject compound (519 mg) as a pale-yellow foamy substance. After completion of the reaction the solvent was distilled off the residue was then dissolved in chloroform by washing with a 1 mol/l sodium hydroxide solution The solution was dried with anhydrous sodium sulfate the solvent was distilled off Subsequently, the residue was dissolved in methanol (6.0 ml) added with 1 mol/l sodium hydroxide by stirring at room temperature for 6 hours After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added the solvent was distilled off After that, ethanol was added to remove insoluble matter the solvent was distilled off the residue was then dried
Source ID: ord-7e25fbcd556647af89095f19b40122f2Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-ab53043f85bf4acc8d31e814fbd29970Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A mixture of methyl 2-cyanobenzoate (1.0 g, 6.2 mmol) and PtO2 (100 mg) in 20 mL EtOH and 1 ml of chloroform was hydrogenated under 50 psi of hydrogen for 2 h. The reaction mixture was filtered through Celite® in a sintered glass funnel and concentrated on a rotary evaporator to give methyl 2-(aminomethyl)benzoate as a HCl salt and this was carried to the next step crude. The reaction mixture was filtered through Celite® in a sintered glass funnel concentrated on a rotary evaporator
Source ID: ord-10aab6ff56c340c5a19daf6a4cf52948Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Commercially available amino methylbenzoic acid methyl ester (manufactured by Tokyo Kasei Kogyo Co., Ltd.) (278 mg) was dissolved in methanol (9 ml). Then, the solution was added with 1-methyl-2-imidazole carboxaldehyde (manufactured by Aldrich Corporation) (407 mg) and sodium cyanoborohydride (317 mg), and then adjusted to about pH 5 with acetic acid, followed by stirring at room temperature for 3 days. After completion of the reaction, the solvent was distilled off and the residue was then dissolved in chloroform, followed by washing with a 1 mol/l sodium hydroxide solution. The solution was dried with anhydrous sodium sulfate, and the solvent was distilled off. Subsequently, the residue was dissolved in methanol (6.0 ml) and then added with 1 mol/l sodium hydroxide, followed by stirring at room temperature for 6 hours. After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added and the solvent was distilled off. After that, ethanol was added to remove insoluble matter, the solvent was distilled off, and the residue was then dried, thereby obtaining the subject compound (519 mg) as a pale-yellow foamy substance. After completion of the reaction the solvent was distilled off the residue was then dissolved in chloroform by washing with a 1 mol/l sodium hydroxide solution The solution was dried with anhydrous sodium sulfate the solvent was distilled off Subsequently, the residue was dissolved in methanol (6.0 ml) added with 1 mol/l sodium hydroxide by stirring at room temperature for 6 hours After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added the solvent was distilled off After that, ethanol was added to remove insoluble matter the solvent was distilled off the residue was then dried
Source ID: ord-d74b1b2bfbb64f849c0b708eede8d9adConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Commercially available amino methylbenzoic acid methyl ester (manufactured by Tokyo Kasei Kogyo Co., Ltd.) (278 mg) was dissolved in methanol (9 ml). Then, the solution was added with 1-methyl-2-imidazole carboxaldehyde (manufactured by Aldrich Corporation) (407 mg) and sodium cyanoborohydride (317 mg), and then adjusted to about pH 5 with acetic acid, followed by stirring at room temperature for 3 days. After completion of the reaction, the solvent was distilled off and the residue was then dissolved in chloroform, followed by washing with a 1 mol/l sodium hydroxide solution. The solution was dried with anhydrous sodium sulfate, and the solvent was distilled off. Subsequently, the residue was dissolved in methanol (6.0 ml) and then added with 1 mol/l sodium hydroxide, followed by stirring at room temperature for 6 hours. After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added and the solvent was distilled off. After that, ethanol was added to remove insoluble matter, the solvent was distilled off, and the residue was then dried, thereby obtaining the subject compound (519 mg) as a pale-yellow foamy substance. After completion of the reaction the solvent was distilled off the residue was then dissolved in chloroform by washing with a 1 mol/l sodium hydroxide solution The solution was dried with anhydrous sodium sulfate the solvent was distilled off Subsequently, the residue was dissolved in methanol (6.0 ml) added with 1 mol/l sodium hydroxide by stirring at room temperature for 6 hours After completion of the reaction, 1 mol/l hydrochloric acid (6.0 ml) was added the solvent was distilled off After that, ethanol was added to remove insoluble matter the solvent was distilled off the residue was then dried
Source ID: ord-7e25fbcd556647af89095f19b40122f2PubChem References
These sources are listed in the compound's public database record.
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