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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292794Generated: October 31, 2026

Water → (1-tert-butyl-5-chloro-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol

https://huagongshe.com/reaction/1292794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant1-tert-butyl-5-chloro-3-trifluoromethyl-1H-pyrazole-4-carboaldehydeHCID 17862922—
SolventMethanolHCID 887—
Product(1-tert-butyl-5-chloro-3-trifluoromethyl-1H-pyrazol-4-yl)-methanolHCID 1786291193.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 39.9 g (156.9 mmoles) of (1-tert-butyl-5chloro-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde dissolved in 300 ml of methanol was cooled to 0° C. Thereto was gradually added 6.5 g (172.6 mmoles) of sodium borohydride. The mixture was stirred at room temperature for 3 hours to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The resulting organic layer was washed with an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain 37.7 g (yield: 93.6%) of (1-tert-butyl-5-chloro-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238689B2
Source datasetuspto-grants-2007_07
ORD IDord-62009966fbb541b6bcfac7bfba06f753
Source noteuspto-grants-2007_07