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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172094Generated: October 25, 2026

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

https://huagongshe.com/reaction/1172094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant5-chloro-1-phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehydeHCID 1479052—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanolHCID 1786291299.9%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 0.21 g (5.5 mmoles) of lithium aluminum hydride dissolved in 70 ml of THF was cooled to −30° C. Thereto was gradually added a solution of 3 g (10.9 mmoles) of 5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazole-4-carboaldehyde dissolved in 30 ml of tetrahydrofuran. The resulting mixture was stirred at −30° C. for 30 minutes to give rise to a reaction. After the completion of the reaction, ethyl acetate was added, followed by stirring. Then, water was added, followed by stirring for a while. The reaction mixture was filtered under vacuum. The filtrate was extracted 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 3.0 g (yield: 99.9%) of (5-chloro-1-phenyl-3-trifluoromethyl-1H-pyrazol-4-yl)-methanol as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-11edac7a272d405db4a49225362489b9
Source noteuspto-grants-2010_11