HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methyl-1-naphthylamine → HCID 13117216, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methyl-1-naphthylamine | HCID 16733 | — |
| Reactant | Butanoic acid, 2-bromo-, methyl ester | HCID 95577 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 13117216 | HCID 13117216 | 86.3% |
Reaction Steps
144.2 g (0.92 mole) of 1-amino-2-methylnaphthalene are stirred with 90.2 g (1.08 moles) of sodium bicarbonate and 507 g (2.8 moles) of methyl 2-bromobutyrate at from 120° to 125° C. for 18 hours. The mixture is cooled, and thereafter the precipitate is filtered off under suction, the filtrate is concentrated under reduced pressure, and the residue is distilled under reduced pressure. 204.3 g (79.5% of theory) of methyl 2-(2-methylnaphth-1-ylamino)-butyrate are obtained as a colorless oil. Boiling point: 148°-150° C./0.25 mbar; nD25 =1.5779.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04568684 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-44e22f9430964bd28edd707b7051e2f2 |
| Source note | uspto-grants-1986_02 |