HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → HCID 57223133, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | HCID 57212777 | HCID 57212777 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57223133 | HCID 57223133 | 79.7% |
Reaction Steps
A mixture of (2R,3S)-3-(4-methoxyphenyl)-2,3-epoxy-N-methylpropionamide (829 mg) and xylene (10 ml) is refluxed with heating under nitrogen atmosphere. When the reflux is started, a solution of 2-aminothiophenol (551 mg) and anhydrous ferric chloride (0.065 mg) in methanol (0.08 ml) is added immediately into the reaction mixture, and the mixture is reacted at the same temperature for 5 minutes, and cooled to room temperature. The precipitated crystals are collected by filtration, washed with xylene, and dried at 60° C. to give (2S,3S)-3-(2-aminophenylthio)-2-hydroxy-3-(4-methoxyphenyl)-N-methylpropionamide (1.06 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05847122 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-768fcba8ce954c978bc4ab04dd6ae1d2 |
| Source note | uspto-grants-1998_12 |