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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691874Generated: November 1, 2026

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

https://huagongshe.com/reaction/1691874

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 numberUS08153644B2
Source datasetuspto-grants-2012_04
ORD IDord-ad4234c99b1e476995e3d3d4c2a15cda
Source noteuspto-grants-2012_04