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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292790Generated: October 25, 2026

Water → (5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol

https://huagongshe.com/reaction/1292790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehydeHCID 17862886—
SolventMethanolHCID 887—
Product(5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanolHCID 17862906106.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1.6 g (41.0 mmoles) of sodium borohydride dissolved in 300 ml of methanol was added, with ice-cooling, a solution of 26.5 g (102.5 mmoles) of 5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde dissolved in 200 ml of methanol. The resulting mixture was stirred at 0° C. for 30 minutes 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 28.5 g (yield: 100%) of (5-fluoro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238689B2
Source datasetuspto-grants-2007_07
ORD IDord-d9bf96384df9442c8a509a389788116a
Source noteuspto-grants-2007_07