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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704499Generated: October 26, 2026

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

https://huagongshe.com/reaction/1704499

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 numberUS04126687
Source datasetuspto-grants-1978_11
ORD IDord-48e2678288b14f4392c962253dfcd6f7
Source noteuspto-grants-1978_11