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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606761Generated: November 3, 2026

Ethanol → 3-[(2-Oxo-2-phenylethyl)thio]-5-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1606761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-ChloroacetophenoneHCID 10757—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 21542284HCID 21542284—
SolventWaterHCID 962—
Product3-[(2-Oxo-2-phenylethyl)thio]-5-(trifluoromethyl)benzoic acidHCID 21544480—

Reaction Steps

A mixture of 1.33 g. (6 m moles) of 3-mercapto-5-trifluoromethylbenzoic acid, 12 ml. of 1N sodium hydroxide solution and 930 mg. (6 m moles) of α-chloroacetophenone in 20 ml. of ethanol is allowed to stir at room temperature for 1 hour. The reaction mixture is diluted with water, extracted with ether and the resulting aqueous phase acidified with 12N hydrochloric acid. The light yellow oil which separates gradually crystallizes and is filtered, 1.8 g., m.p. 135°-150° C. A sample is sublimed at 165° C. and 0.05 mm pressure, m.p. 153°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953595
Source datasetuspto-grants-1976_04
ORD IDord-e36e3b0729484a2ea375cfaa31e9e3ec
Source noteuspto-grants-1976_04