HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Acetylamino-alpha-tolylthiophenylacetic acid → N-Acetyl-DL-phenylglycine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Acetylamino-alpha-tolylthiophenylacetic acid | HCID 86733267 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-Acetyl-DL-phenylglycine | HCID 85935 | 73% |
Reaction Steps
Two (2.0) cc of Raney nickel (WII) was suspended in 15 ml of acetone, and refluxed for 7 minutes. Cooling the suspension to room temperature, 315 mg of α-acetylamino-α-tolylthiophenylacetic acid was added, followed by 5.5 hours' stirring at room temperature. The insoluble matter was separated by filtration, and washed with ethanol. The filtrate and washing were combined and concentrated under reduced pressure. The residue was crystallized from an ether-n-hexane system. Thus 141 mg of α-acetylaminophenylacetic acid was obtained. The yield was 73%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03952044 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-386f7d6536084da18b1ad9a9baae91ff |
| Source note | uspto-grants-1976_04 |