Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641795Generated: November 1, 2026

Sodium Hydroxide → 1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/1641795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1-phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 11448972—
SolventMethanolHCID 887—
Product1-Phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acidHCID 1496824589%

Reaction Steps

A mixture of 1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester (1.25 g, 4.4 mmol) and 1N aqueous sodium hydroxide solution (17.3 mL) in methanol (20 mL) was stirred at room temperature overnight. The reaction mixture was concentrated and acidified to pH ˜1 with 1N aqueous hydrochloric acid. The slurry was extracted with methylene chloride and the combined organic layers were washed with saturated sodium chloride and dried over sodium sulfate. Filtration and concentration gave 1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (1 g, 89% yield) as an off-white solid, which was directly used in the next step without further purification. LCMS calcd for C11H7F3N2O2 (m/e) 256, obsd 255 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115011B2
Source datasetuspto-grants-2012_02
ORD IDord-5344087abc3c4f02a0bdf8657de3b644
Source noteuspto-grants-2012_02