HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorobenzene → HCID 57060229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | HCID 57063652 | HCID 57063652 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57060229 | HCID 57060229 | 73.7% |
Reaction Steps
A mixture of (2R,3S)-3-(4-methoxyphenyl)-2,3-epoxy-N-phenylpropionamide (539 mg) and chlorobenzene (5 ml) is refluxed with heating under nitrogen atmosphere. When the reflux is started, a solution of 2-aminothiophenol (275 mg) and ferric chloride hexahydrate (0.054 mg) in methanol (0.1 ml) is added immediately to the reaction mixture. The mixture is stirred at the same temperature for 5 minutes, and cooled to room temperature. The precipitated crystals are collected by filtration, washed with chlorobenzene, and dried at 50° C. to give (2S,3S)-3-(2-aminophenylthio)-2-hydroxy-3-(4-methoxyphenyl)-N-phenylpropionamide (582 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05847122 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-8825a0019ae74d969ff0f0f7454027d2 |
| Source note | uspto-grants-1998_12 |