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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090829Generated: November 2, 2026

2-(Chloromethyl)aniline--hydrogen chloride (1/1) → 2-(2-Aminobenzylthio)imidazole

https://huagongshe.com/reaction/1090829

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Chloromethyl)aniline--hydrogen chloride (1/1)HCID 12387941—
ReactantHCID 178527877HCID 178527877—
SolventEthanolHCID 702—
Product2-(2-Aminobenzylthio)imidazoleHCID 1502742081.2%

Reaction Steps

To a solution of 1.5 g (15 mmol) of 2-mercaptoimidazole in 15 ml of ethanol was added at room temperature 2.66 g (15 mmol) of 2-aminobenzyl chloride hydrochloride. The mixture was then stirred for one hr. at room temperature. The obtained homogeneous solution was placed under reduced pressure at a temperature below 40° C. to distill off the solvent. To the residue were successively added water and saturated aqueous sodium hydrogencarbonate to precipitate a crystalline product. The product was collected by filtration, washed twice with water, and dried to give 2.5 g of the desired compound as a pale gray crystalline product, yield 80.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05082943
Source datasetuspto-grants-1992_01
ORD IDord-4a1dcffda9f544599cc9fd18e9fb909d
Source noteuspto-grants-1992_01