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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833630Generated: October 26, 2026

Thionyl Chloride → 5-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1833630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-oneHCID 3017358—
SolventChloroformHCID 6212—
Product5-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 20385630—

Reaction Steps

A mixture of 20 parts of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one, 34 parts of sulfinyl chloride and 300 parts of trichloromethane is stirred and refluxed for 4 hours. The trichloromethane is evaporated and the residue is crystallized from 4-methyl-2-pentanone (activated charcoal). The product is filtered off (the filtrate is set aside), yielding a first fraction of 8.2 parts of 5-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one. The filtrate, which was set aside, is concentrated and the concentrate is stirred with 2,2'-oxybispropane. The precipitated product is filtered off and dried, yielding a second fraction of 8 parts of 5-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066772
Source datasetuspto-grants-1978_01
ORD IDord-6633218ba4494898a80e47d25064d2d0
Source noteuspto-grants-1978_01