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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22557Generated: October 30, 2026

Thionyl Chloride → 5-(3-chloropropyl)-1-(alpha-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole hydrochloride

https://huagongshe.com/reaction/22557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant1-(alpha-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole-5-propanolHCID 19930417—
SolventDichloromethaneHCID 6344—
Product5-(3-chloropropyl)-1-(alpha-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole hydrochlorideHCID 19930415—

Reaction Steps

To a solution of 5.75 g of thionylchloride in 80 ml of methylene chloride is added 8.4 g of 1-(α-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole-5-propanol as a solid in portions. When addition is complete, the solution is refluxed for 1.5 h, cooled in ice and filtered to obtain 5-(3-chloropropyl)-1-(α-ethoxycarbonyl-p-cyanobenzyl)-1H-imidazole hydrochloride. The salt is partitioned between methylene chloride and saturated sodium bicarbonate. The organic extracts are washed with water, dried over sodium sulfate and evaporated to yield the free base.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428160
Source datasetuspto-grants-1995_06
ORD IDord-569d8cfa8411410f8eb962716f476b63
Source noteuspto-grants-1995_06