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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376435Generated: October 25, 2026

Water → 1-(4-Fluoro-3-cyanophenyl)-3-trifluoromethyl-5-hydroxymethylpyrazole

https://huagongshe.com/reaction/376435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(4-Fluoro-3-cyanophenyl)-3-trifluoromethyl-5-bromomethylpyrazoleHCID 22280795—
CatalystHCID 178419072HCID 178419072—
SolventDimethyl SulfoxideHCID 679—
Product1-(4-Fluoro-3-cyanophenyl)-3-trifluoromethyl-5-hydroxymethylpyrazoleHCID 22280740—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-(3-cyano-4-fluorophenyl)-3-trifluoromethyl-5-bromomethyl pyrazole(2.5 g, 7.18 mmol) in DMSO (40 mL) was added copper(I) oxide(2.16 g, 15.08 mmol) and water (12 mL). The reaction mixture was stirred at 60° C. for 2 hours then cooled to RT and stirred at RT overnight. The next day, the mixture was filtered through celite, filter pad was washed with ethyl acetate(20 mL); the filtrate was partitioned between ethyl acetate(50 mL) and water(50 mL); organic phase was separated and washed with water(3×30 mL); dried over sodium sulfate; filtered, concentrated, flash chromatography (ethyl acetate : hexane, 1:6) to afford 1-(3-cyano-4-fluorophenyl)-3-trifluoromethyl-5-hydroxymethyl pyrazole(1.7 g). CI mass spectrum m/z (rel. intensity) 286 (M+H, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020357
Source datasetuspto-grants-2000_02
ORD IDord-db60bfc85dff428f94cba57dd6b8eb3a
Source noteuspto-grants-2000_02