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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457264Generated: November 1, 2026

Chlorobenzene → HCID 57060229, compound

https://huagongshe.com/reaction/1457264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
Reactant2-AminothiophenolHCID 8713—
ReactantHCID 57063652HCID 57063652—
SolventMethanolHCID 887—
ProductHCID 57060229HCID 5706022973.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05847122
Source datasetuspto-grants-1998_12
ORD IDord-8825a0019ae74d969ff0f0f7454027d2
Source noteuspto-grants-1998_12