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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292809Generated: October 30, 2026

Water → (5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazol-4-yl)methanol

https://huagongshe.com/reaction/1292809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 19754692—
SolventMethanolHCID 887—
Product(5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazol-4-yl)methanolHCID 1786287152.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 7.2 g (37.0 mmoles) of 5-chloro-3-difluoromethyl-1-methyl-1H-pyrazole-4-carboaldehyde dissolved in 100 ml of methanol was cooled to 0° C. Thereto was gradually added 2.1 g (55.5 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 3.8 g (yield: 52.1%) of (5-chloro-3-difluoromethyl-1-methyl-1H-pyrazol-4-yl)-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238689B2
Source datasetuspto-grants-2007_07
ORD IDord-d6c664937e5a44c08ddea4cb267a9a43
Source noteuspto-grants-2007_07