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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913766Generated: November 2, 2026

Thionyl Chloride → 4-(4-Trifluoromethylphenyl)benzylchloride

https://huagongshe.com/reaction/1913766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(4'-(Trifluoromethyl)-[1,1'-biphenyl]-4-yl)methanolHCID 22015014—
SolventChloroformHCID 6212—
Product4-(4-Trifluoromethylphenyl)benzylchlorideHCID 1145992198%

Reaction Steps

2.89 ml (39.65 mmol) of thionyl chloride dissolved in 10 ml of chloroform are added to a solution of 5.0 g (19.82 mmol) of (4′-trifluoromethylbiphenyl-4-yl)methanol in 40 ml of chloroform, and the mixture is stirred at room temperature for 12 hours. After reaction is complete, the reaction mixture is evaporated to dryness, and the residue is taken up in ethyl acetate and washed with saturated sodium carbonate solution. The organic phase is separated off, dried over sodium sulphate and evaporated 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% yield) of a colourless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609727B2
Source datasetuspto-grants-2013_12
ORD IDord-094c11a69d28425baccba49efd3ec264
Source noteuspto-grants-2013_12