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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177507Generated: November 3, 2026

Sodium Hydroxide → 2-Cyclopropyl-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/2177507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-cyclopropyl-4-(trifluoromethyl)benzoateHCID 59438487—
SolventEthanolHCID 702—
Product2-Cyclopropyl-4-(trifluoromethyl)benzoic acidHCID 5943848543.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 485 mg (1.986 mmol) 2-cyclopropyl-4-trifluoromethyl-benzoic acid methyl ester in 8 ml ethanol at room temperature, was added 1.99 ml (3.972 mmol) 2N NaOH. The mixture was heated in an 80° C. oil bath for 30 minutes. The solution was cooled to room temperature and the ethanol was evaporated. The residue was diluted with water, acidified with 2N HCl to pH 2 and dichloromethane was added. The aqueous phase was extracted twice with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified on silica gel (Eluent: Heptane/ethyl acetate 0 to 100%) to provide 0.197 g (27%) of the title compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067911B2
Source datasetuspto-grants-2015_06
ORD IDord-f10306c4300d4f55ae068b859d18d2c5
Source noteuspto-grants-2015_06