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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172101Generated: November 3, 2026

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

https://huagongshe.com/reaction/1172101

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-5-chloro-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 numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-d22e83676ec64950b06ebb9ac5e78863
Source noteuspto-grants-2010_11