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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413470Generated: October 27, 2026

Thionyl Chloride → 5-chloro-1-(3-chloropropyl)-2-cyclohexyl-1H-benzimidazole hydrochloride

https://huagongshe.com/reaction/1413470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-chloro-2-cyclohexyl-1H-benzimidazole-1-propanolHCID 13105617—
SolventChloroformHCID 6212—
Product5-chloro-1-(3-chloropropyl)-2-cyclohexyl-1H-benzimidazole hydrochlorideHCID 20506333—

Reaction Steps

To a stirred mixture of 21 parts of 5-chloro-2-cyclohexyl-1H-benzimidazole-1-propanol in 225 parts of trichloromethane are added dropwise 40 parts of sulfinyl chloride (exothermic reaction). Upon completion, stirring is continued for 2 hours at reflux temperature. The reaction mixture is evaporated and the residue is dissolved in boiling water. The solution is treated with activated charcoal. The latter is filtered off till a clear filtrate is obtained. After cooling in an ice-bath, the precipitated product is filtered off and dried, yielding 5-chloro-1-(3-chloropropyl)-2-cyclohexyl-1H-benzimidazole hydrochloride; mp. 211.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250176
Source datasetuspto-grants-1981_02
ORD IDord-2110b0b93c664affafdc89689a868da1
Source noteuspto-grants-1981_02