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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629408Generated: October 30, 2026

Thionyl Chloride → 1-(4-(chloromethyl)-3-fluorophenyl)-1H-pyrazole

https://huagongshe.com/reaction/629408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(2-fluoro-4-(1H-pyrazol-1-yl)phenyl)methanolHCID 59028616—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product1-(4-(chloromethyl)-3-fluorophenyl)-1H-pyrazoleHCID 59028599—

Reaction Steps

To a solution of (2-fluoro-4-(1H-pyrazol-1-yl)phenyl)methanol (0.71 g) in THF (15.0 mL) was added thionyl chloride (0.40 mL) under ice-cooling, and the mixture was stirred at room temperature for 16 hr. The reaction mixture was diluted with ethyl acetate, saturated aqueous sodium bicarbonate was added thereto, and the mixture was partitioned. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (0.50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315458B2
Source datasetuspto-grants-2016_04
ORD IDord-4d3dc858a8384f9bb1f0238fb4487f11
Source noteuspto-grants-2016_04