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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435652Generated: October 28, 2026

Ethanol → 2-Phenylthio-5-trifluoromethylbenzoic acid

https://huagongshe.com/reaction/435652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant2-(Phenylthio)-5-(trifluoromethyl)benzonitrileHCID 1489521—
SolventWaterHCID 962—
Product2-Phenylthio-5-trifluoromethylbenzoic acidHCID 104231—

Reaction Conditions

Temperature0 °C

Reaction Steps

6 g of 2-(phenylthio)-5-trifluoromethyl-benzonitrile, 40 ml of 15% aqueous sodium hydroxide solution and 12 ml of ethanol are heated under reflux for 12 hours and then cooled. After the addition of 100 ml of water, the mixture is extracted with 80 ml of benzene. The aqueous phase is cooled to 0° C and acidified with concentrated hydrochloric acid. The precipitate which separates out is extracted with methylene chloride. The organic phase is washed with water until neutral, dried over sodium sulphate, filtered and evaporated. There is obtained 2-(phenylthio)-5-trifluoromethyl-benzoic acid which melts at 140°-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04006145
Source datasetuspto-grants-1977_02
ORD IDord-808760e5b6ba4c0c9333276f1be42940
Source noteuspto-grants-1977_02