HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 2-Amino-5-cyano-N,3-dimethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 25156989 | HCID 25156989 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-5-cyano-N,3-dimethylbenzamide | HCID 25157282 | 80.3% |
Reaction Steps
Methylamine (117 g, 3.77 mol) is introduced into a solution of ethyl 2-amino-5-cyano-3-methylbenzoate (50 g, 0.251 mol) in methanol (175 mL), sodium methoxide (1.13 g, 30% strength in methanol, 6.28 mmol) is added and the reaction mixture is stirred overnight at room temperature. Thereafter, 100 ml of 22% strength NaOH are added and the batch is cooled down to 10° C. The suspension obtained is filtered and the solid obtained is washed once with 1:1 methanol:water and then with 50 mL of water. The solid is dried at 50° C. in a vacuum drying cabinet. 2-Amino-5-cyano-N,3-dimethylbenzamide is isolated as a slightly beige solid. Yield: 80.3% of theory, purity: 94.9% quantitative LC, 73 ppm Cu).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169198B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-6a2c66001ead48ef97ee76ddbc926ccd |
| Source note | uspto-grants-2015_10 |