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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39425Generated: October 26, 2026

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

https://huagongshe.com/reaction/39425

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. MS (m/e): 229.0 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524909B2
Source datasetuspto-grants-2013_09
ORD IDord-513a2865dc3247a8bbc54ea1d3089d65
Source noteuspto-grants-2013_09