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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1690274Generated: October 26, 2026

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

https://huagongshe.com/reaction/1690274

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 numberUS08153653B2
Source datasetuspto-grants-2012_04
ORD IDord-c2d8fa6ab09f4345879d6893e057278a
Source noteuspto-grants-2012_04