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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660443Generated: October 26, 2026

Methyl 2-phenylthio-2-(3-phenoxyphenyl)propionate → Methyl 2-(3-phenoxyphenyl)propanoate

https://huagongshe.com/reaction/1660443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-phenylthio-2-(3-phenoxyphenyl)propionateHCID 20556693—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductMethyl 2-(3-phenoxyphenyl)propanoateHCID 52908290.7%

Reaction Steps

Methyl α-phenylthio-α-(m-phenoxyphenyl)propionate (210 mg) was dissolved in 1 ml of ethanol. An ethanol suspension (5 ml) of 2 cc of Raney nickel (W-II) was added, and the mixture was stirred at room temperature for 5 hours. The reaction mixture was filtered, and the insoluble matter was washed with 50 ml of methanol. The filtrate and the washing were combined, and concentrated under reduced pressure. Methylene chloride (30 ml) was added to the residue, and the insoluble matter was separated by filtration. The filtrate was concentrated under reduced pressure, and the residue was chromatographed on a column of silica gel using benzene as an eluent to afford 134 mg of methyl α-(m-phenoxyphenyl)propionate in a yield of 90%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308208
Source datasetuspto-grants-1981_12
ORD IDord-dedbc46eab914c4281132550406ff922
Source noteuspto-grants-1981_12