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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189767Generated: October 30, 2026

Water → 4-Cyclohexyl-3-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/2189767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Cyclohexyl-3-(trifluoromethyl)benzamideHCID 59201794—
SolventEthanolHCID 702—
Product4-Cyclohexyl-3-(trifluoromethyl)benzoic acidHCID 5743003389.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-cyclohexyl-3-(trifluoromethyl)benzamide (D33) (822 mg, 3.03 mmol) in ethanol (40 ml) was added potassium hydroxide (1.700 g, 30.3 mmol) and water (5 ml) and the reaction heated to 90° C. block temperature for 3 h and stirred at room temperature for 16 h. Further potassium hydroxide (1.700 g, 30.3 mmol) was added and the reaction heated at reflux for 27 h. A further 5 mL of water was added and the reaction heated for 66 hours (weekend). The reaction mixture was concentrated in vacuo and the residue partitioned between ethyl acetate (25 mL) and aqueous hydrochloric acid (2M, 25 mL). The aqueous layer was further extracted with ethyl acetate (25 mL) and the combined organic phases dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound as a white solid (737 mg). MS (ES): C14H15F3O2 requires 272; found 271 (M−H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324254B2
Source datasetuspto-grants-2012_12
ORD IDord-fa70763c5afa4c34818c679094a8bad3
Source noteuspto-grants-2012_12