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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068441Generated: October 26, 2026

Thionyl Chloride → 1-(4-Cyanobenzyl)-5-chloromethyl-2-methylimidazole hydrochloride salt

https://huagongshe.com/reaction/1068441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-(4-Cyanobenzyl)-5-hydroxymethyl-2-methylimidazoleHCID 21193415—
Product1-(4-Cyanobenzyl)-5-chloromethyl-2-methylimidazole hydrochloride saltHCID 21193348—

Reaction Steps

A mixture of 1-(4-cyanobenzyl)-5-hydroxymethyl-2-methylimidazole (3.45 g, 15.2 mmol) and thionyl chloride (30 mL, 411 mmol) was stirred at room temp. overnight under a calcium chloride drying tube. The resultant mixture was concentrated under vacuum, and residual thionyl chloride was removed by co-evaporation with toluene. The residue was triturated with anhydrous diethyl ether, filtered, washed with ether to provide the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248756B1
Source datasetuspto-grants-2001_06
ORD IDord-4ac8f2a410e64afbb3e389b1be355637
Source noteuspto-grants-2001_06