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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914452Generated: November 1, 2026

Thionyl Chloride → 4-(chloromethyl)-1-phenyl-1H-pyrazole

https://huagongshe.com/reaction/914452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant(1-phenyl-1H-pyrazol-4-yl)methanolHCID 822983—
SolventDichloromethaneHCID 6344—
Product4-(chloromethyl)-1-phenyl-1H-pyrazoleHCID 2121162106.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

(1-Phenyl-1H-pyrazol-4-yl)methanol (6.3 g) synthesized in Reference Example 17 was dissolved in dichloromethane (100 mL) and, after ice-cooling, thionyl chloride (5.59 g) was added thereto, and the mixture was stirred at 0° C. for 2 hr. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture, and the mixture was extracted with dichloromethane. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (elution solvent; hexane:ethyl acetate=4:1) to give the title compound (7.4 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026370B2
Source datasetuspto-grants-2011_09
ORD IDord-14b05bdfa4cf48ae9e5231de0184d5cc
Source noteuspto-grants-2011_09