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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833662Generated: October 26, 2026

Thionyl Chloride → Benzimidazole, 1-(4-chlorobutyl)-

https://huagongshe.com/reaction/1833662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1h-Benzimidazole-1-butanolHCID 20506323—
SolventChloroformHCID 6212—
ProductBenzimidazole, 1-(4-chlorobutyl)-HCID 58317045%

Reaction Steps

To a stirred mixture of 50 parts of 1H-benzimidazole-1-butanol and 375 parts of trichloromethane are added dropwise 35.2 parts of sulfinyl chloride. Upon completion, stirring is continued for 3 hours at reflux temperature. The reaction mixture is evaporated. The residue is taken up in trichloromethane. The whole is washed with ammonium hydroxide and the solvent is evaporated. The residue is purified by column-chromatography over silica gel using trichloromethane as eluent. The pure fractions are collected and the eluent is evaporated, yielding 22 parts (45%) of 1-(4-chlorobutyl)-1H-benzimidazole as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066772
Source datasetuspto-grants-1978_01
ORD IDord-505b4e2e99be46849e95ccb6ceb19e45
Source noteuspto-grants-1978_01