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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638559Generated: October 26, 2026

Thionyl Chloride → HCID 14722476, compound

https://huagongshe.com/reaction/1638559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-(4-Nitrobenzyl)-2-hydroxymethylbenzimidazoleHCID 14722475—
SolventChloroformHCID 6212—
ProductHCID 14722476HCID 14722476—

Reaction Steps

To a solution of 2.2 g 1-(4-nitrobenzyl)-2-hydroxymethylbenzimidazole in 30 mL of chloroform was added 3.3 mL of thionyl chloride. The reaction mixture was stirred at room temperature for 18 hours and then concentrated in vacuo. The residue was taken up in water, neutralized with K2CO3 to a pH of 10 and extracted into methylene chloride. The organic layer was dried over Na2SO4 and concentrated to give 2 g of 1-(4-nitrobenzyl)-2-chloromethylbenzimidazole as a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880804
Source datasetuspto-grants-1989_11
ORD IDord-d06229224082413db601a69d10cbacb4
Source noteuspto-grants-1989_11