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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413464Generated: October 27, 2026

Thionyl Chloride → HCID 20506327, compound

https://huagongshe.com/reaction/1413464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-chloro-2-(phenylmethyl)-1H-benzimidazole-1-propanolHCID 20506270—
SolventChloroformHCID 6212—
ProductHCID 20506327HCID 20506327—

Reaction Steps

To a stirred mixture of 45 parts of 5-chloro-2-(phenylmethyl)-1H-benzimidazole-1-propanol and 225 parts of trichloromethane are added dropwise 29.75 parts of sulfinyl chloride. Upon completion, stirring is continued for 6 hours at reflux temperature. The reaction mixture is evaporated and the residue is taken up in water. The product is extracted with trichloromethane. The extract is dried, filtered and evaporated. The reisude is purified by columnchromatography over silica gel using a mixture of trichloromethane and methanol (98:2) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 5-chloro-1-(3-chloropropyl)-2-(phenylmethyl)-1H-benzimidazole as a solid residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250176
Source datasetuspto-grants-1981_02
ORD IDord-7bd6c6e079b9434c95ce609cc3386619
Source noteuspto-grants-1981_02