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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12822Generated: October 26, 2026

Lithium Hydroxide → 1-tert-Butyl-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/12822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantEthyl 1-(tert-butyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 2782985—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-tert-Butyl-5-(trifluoromethyl)-1H-pyrazole-4-carboxylic acidHCID 148203980.3%

Reaction Steps

To a solution of 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester (5 g, 21.2 mmol, purchased from Bionet) in CH3OH (45 mL) and water (45 mL) was added LiOH (0.54 g, 22.5 mmol). The reaction mixture was stirred at reflux for 4 h, and then the solution was concentrated under reduced pressure to remove the methanol. The residue was diluted with water and the solution was acidified to pH 2 with concentrated HCl. The resulting mixture was then extracted with ethyl acetate three times. The combined organic extracts were concentrated in vacuo to give 1-tert-butyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid (4.02 g, 80%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728029B2
Source datasetuspto-grants-2010_06
ORD IDord-7c97ea2069d945458aadd4baa1d276b4
Source noteuspto-grants-2010_06