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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921871Generated: October 30, 2026

Thionyl Chloride → 4-(4-Trifluoromethylphenyl)benzylchloride

https://huagongshe.com/reaction/1921871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(4'-(Trifluoromethyl)-[1,1'-biphenyl]-4-yl)methanolHCID 22015014—
SolventChloroformHCID 6212—
Product4-(4-Trifluoromethylphenyl)benzylchlorideHCID 11459921—

Reaction Steps

A solution of 5.00 g (19.8 mmol) of (4′-trifluoromethylbiphenyl-4-yl)methanol in 40 ml of chloroform is mixed with 2.89 ml (39.7 mmol) of thionyl chloride dissolved in 10 ml of chloroform, and the mixture is stirred at room temperature over 12 hours. After reaction is complete, the reaction mixture is concentrated to dryness, and the residue is taken up ethyl acetate and washed with saturated sodium carbonate solution. The organic phase is subsequently separated off, dried over sodium sulfate and concentrated after filtration. The resulting crude product is purified by flash chromatography on silica gel 60 (mobile phase: cyclohexane/ethyl acetate 9:1). 5.26 g (19.4 mmol, 98% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173704B2
Source datasetuspto-grants-2012_05
ORD IDord-3f4f417d7ea64f87a4e6c1819f5bc278
Source noteuspto-grants-2012_05