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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413466Generated: October 27, 2026

Thionyl Chloride → HCID 20506324, compound

https://huagongshe.com/reaction/1413466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-chloro-2-methyl-1H-benzimidazole-1-propanolHCID 20506357—
SolventChloroformHCID 6212—
ProductHCID 20506324HCID 20506324—

Reaction Steps

To a stirred mixture of 6.5 parts of 5-chloro-2-methyl-1H-benzimidazole-1-propanol and 120 parts of trichloromethane are added dropwise 12 parts of sulfinyl chloride. Upon completion, the whole is heated to reflux and stirring is continued for 3 hours at reflux temperature. The reaction mixture is cooled and evaporated. Water is added to the residue and the mixture is treated with activated charcoal. The latter is filtered off and the filtrate is alkalized with ammonium hydroxide. The product is extracted with trichloromaethane. The extract is dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding 5-chloro-1-(3-chloropropyl)-2-methyl-1H-benzimidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250176
Source datasetuspto-grants-1981_02
ORD IDord-354cc80368e7480f9bc4816180796507
Source noteuspto-grants-1981_02