HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Acetamide, N-[(1R)-2-(4-methoxyphenyl)-1-methylethyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | (+-)-p-Methoxyamphetamine | HCID 31721 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Acetamide, N-[(1R)-2-(4-methoxyphenyl)-1-methylethyl]- | HCID 11769683 | — |
Reaction Steps
In 6 ml of pyridine was dissolved 1.5 g of (-)-2-(p-methoxyphenyl)-1-methylethylamine ([α]D23 : -30.1° (c=1.2, methanol)), and after adding thereto 3 ml of acetic anhydride, the mixture was allowed to stand at room temperature for 1 hour. After distilling off the solvent, the residue was extracted with ethyl acetate. The ethyl acetate extract was washed with water, and dried over anhydrous sodium sulfate, and the solvent was distilled off and the crude crystals formed were recrystallized from a mixture of n-hexane and benzene to provide 1.8 g of (R)(+)-N-acetyl-2-(p-methoxyphenyl)-1-methylethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04731478 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-3734550b42de4d38bc1e22804a036c25 |
| Source note | uspto-grants-1988_03 |