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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927417Generated: November 2, 2026

Thionyl Chloride → 4-(4-Trifluoromethylphenyl)benzylchloride

https://huagongshe.com/reaction/1927417

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 5.0 g (19.82 mmol) of (4′-trifluoromethylbiphenyl-4-yl)methanol in 40 ml of chloroform is mixed with 2.89 ml (39.65 mmol) of thionyl chloride dissolved in 10 ml of chloroform, and the mixture is stirred at room temperature for 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 (mobile phase: cyclohexane/ethyl acetate 9:1). 5.26 g (19.43 mmol, 98% of theory) of a colorless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183271B2
Source datasetuspto-grants-2012_05
ORD IDord-f76a4a43de644289a20bab8980354be1
Source noteuspto-grants-2012_05