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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276897Generated: October 31, 2026

Thionyl Chloride → 1h-Benzimidazole,6-(chloromethyl)-1-[(2-chlorophenyl)methyl]-2-methyl-,hydrochloride

https://huagongshe.com/reaction/1276897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1h-Benzimidazole-6-methanol,1-[(2-chlorophenyl)methyl]-2-methyl-HCID 18315538—
Product1h-Benzimidazole,6-(chloromethyl)-1-[(2-chlorophenyl)methyl]-2-methyl-,hydrochlorideHCID 22620341—

Reaction Steps

Five milliliters of thionyl chloride were added to 3.56 g of 1-(2-chlorobenzyl)-6-hydroxymethyl-2-methylbenzimidazole, and the mixture was stirred at room temperature for 20 minutes and then at 80° C. for 20 minutes. After excess thionyl chloride was distilled off under reduced pressure, the residue was dissolved in 10 ml of chloroform, and the solution was crystallized from hexane. The crystals were separated through filtration, washed with hexane, and dried to give 4.07 g of 1-(2-chlorobenzyl)-6-chloromethyl-2-methylbenzimidazole hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166219
Source datasetuspto-grants-2000_12
ORD IDord-1c878082e4884f07a3867e8d34a67d1a
Source noteuspto-grants-2000_12