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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3244Generated: October 26, 2026

5,5-Dimethyl-2,4-imidazolidinedithione → 2,4-bis(2-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole

https://huagongshe.com/reaction/3244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,5-Dimethyl-2,4-imidazolidinedithioneHCID 3002142—
Reactant2-(chloromethyl)-N,N-dimethylaniline hydrochlorideHCID 13537426—
SolventEthanolHCID 702—
Product2,4-bis(2-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazoleHCID 18934848—

Reaction Steps

Initially, a solution of 9.1 g of 2-dimethylaminobenzylchloride hydrochloride in 50 mL of EtOH was added to a solution of 7 g of 5,5-dimethyl-2,4-dithiohydantoin in 100 mL of ethanol (EtOH). The reaction mixture was stirred for 1.5 hour at the room temperature and concentrated in vacuo. To the residue, there was added 100 mL of chloroform (CHCl3). The residue was then washed with an aqueous solution of potassium carbonate (CaCO3), dried over magnesium sulfate (MgSO4), and concentrated in vacuo. The residue was chromatographed on a column of silica gel (CHCl3). From the earlier fractions, 2,4-bis(2-dimethylaminobenzylthio)-5,5-dimethyl-5H-imidazole was isolated as a syrup. The yield of this compound was 1.1 g with a yield ratio of 5.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05733922
Source datasetuspto-grants-1998_03
ORD IDord-a4c2572338d149fc9b4505fc6cb945cf
Source noteuspto-grants-1998_03