Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2350863Generated: November 1, 2026

2-Ethylaminobenzyl bromide hydrobromide → 2-(2-Ethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazole

https://huagongshe.com/reaction/2350863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethylaminobenzyl bromide hydrobromideHCID 19847389—
ReactantHCID 178527818HCID 178527818—
SolventAcetoneHCID 180—
Product2-(2-Ethylaminobenzylmercapto)-1H-thieno[3,4-d]imidazoleHCID 14181149—

Reaction Steps

1.12 g of 2-ethylaminobenzyl bromide hydrobromide are added to a solution of 0.60 g of 2-mercaptothieno-[3,4-d]imidazole in 100 ml of acetone. After the mixture has been stirred at room temperature for 24 hours, the solvent is removed by distillation in vacuo, and the crystalline residue is washed with acetone. Then 1N NH4OH solution is added to the product, the mixture is stirred for 2 hours, and the solid is filtered off with suction and washed wit water. The residue which has been dried in air is dissolved in methylene chloride, active charcoal is added, and the mixture is filtered. Concentration in vacuo results in the clorless crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871734
Source datasetuspto-grants-1989_10
ORD IDord-c3da992faa2e434ca5fd5483bc36f024
Source noteuspto-grants-1989_10