Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082674Generated: November 1, 2026

Thionyl Chloride → 3-Trifluoromethylbenzhydryl chloride

https://huagongshe.com/reaction/2082674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-(Trifluoromethyl)benzhydrolHCID 2777404—
SolventChloroformHCID 6212—
Product3-Trifluoromethylbenzhydryl chlorideHCID 596829100%

Reaction Steps

To a stirred mixture of 40 parts of sulfinyl chloride in 150 parts of trichloromethane is added dropwise a solution of 64 parts of α-phenyl-3-(trifluoromethyl)benzenemethanol in 375 parts of trichloromethane. Upon completion, stirring is continued for 1 hour at room temperature. The whole is heated to reflux and stirring is continued for 3 hours at reflux temperature. After stirring overnight at room temperature, the solvent is evaporated. The residue is taken up in methylbenzene and the latter is evaporated again, yielding 70 parts (100%) of 1-(chlorophenylmethyl)-3-(trifluoromethyl)benzene as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082755
Source datasetuspto-grants-1978_04
ORD IDord-83a79e8b53454c84ae64437917732ccd
Source noteuspto-grants-1978_04