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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704466Generated: October 30, 2026

Methane → 6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1704466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantThionyl ChlorideHCID 24386—
Reactant6-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-oneHCID 20385651—
SolventChloroformHCID 6212—
Product6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 2038558777.5%

Reaction Steps

To a stirred mixture of 22.6 parts of 6-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one and 300 parts of trichloromethane are added dropwise 32 parts of sulfinyl chloride. Upon completion, stirring is continued for 3 hours at reflux. After stirring with activated charcoal, the reaction mixture is filtered hot over hyflo. The filtrate is evaporated and the residue is dissolved in methylbenzene. The solution is washed a few times with water, dried, filtered and evaporated. The oily residue is triturated in 2,2'-oxybispropane. The solid product is filtered off and dried, yielding 19 parts (77.5%) of 6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one; mp. 122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126687
Source datasetuspto-grants-1978_11
ORD IDord-09166e12c079483cb5588d2d3602c9a7
Source noteuspto-grants-1978_11