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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732456Generated: November 2, 2026

Methanol → alpha-Methylthio-alpha-(m-phenoxyphenyl)propionic acid

https://huagongshe.com/reaction/1732456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl alpha-methylthio-alpha-(m-phenoxyphenyl)propionateHCID 12917662—
SolventWaterHCID 962—
Productalpha-Methylthio-alpha-(m-phenoxyphenyl)propionic acidHCID 1291767299.3%

Reaction Steps

Methanol (4 ml) and 2 ml of water were added to 663 mg of methyl α-methylthio-α-(m-phenoxyphenyl)propionate, and then 300 mg of sodium hydroxide was added. The mixture was heated under reflux for 2 hours. The mixture was diluted with 30 ml of water, and extracted with 10 ml of diethyl ether. The aqueous layer was acidified with about 1 ml of conc. hydrochloric acid, and extracted three times with 20 ml of diethyl ether. The organic layer was washed with 10 ml of water, and dried over anhydrous sodium sulfate. Concentration under reduced pressure gave 628 mg of α-methylthio-α-(m-phenoxyphenyl)propionic acid as an oil in a yield of 99%. This product crystallized on standing at room temperature. Recrystallization from hexane/carbon tetrachloride afforded colorless crystals having a melting point of 87° to 88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237298
Source datasetuspto-grants-1980_12
ORD IDord-8bd42bf604894618a2dda91e92195b9c
Source noteuspto-grants-1980_12