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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646704Generated: October 31, 2026

m-Chloroperbenzoic acid → 2-(2-Aminobenzylsulfinyl)imidazole

https://huagongshe.com/reaction/1646704

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-(2-Aminobenzylthio)imidazoleHCID 15027420—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product2-(2-Aminobenzylsulfinyl)imidazoleHCID 1502742112.7%

Reaction Steps

To a solution of 2.5 g of 2-(2-aminobenzylthio)imidazole in a mixture of 25 ml of chloroform and 10 ml of methanol was dropwise added under stirring and under chilling with ice 2.6 g (12.1 mmol) of m-chloroperbenzoic acid. The mixture was further stirred for 15 min. Thus precipitated crystalline product was collected by filtration, washed twice with water and placed in 40 ml of saturated aqueous sodium hydrogencarbonate. The aqueous mixture was stirred, and then the crystalline product was collected by filtration. The obtained solid product was stirred in a mixture of 30 ml of chloroform and 10 ml of 1N aqueous NaOH. The aqueous portion was taken out and made ammonia-alkaline by addition of 20% aqueous ammonium chloride. The mixture was chilled after addition of sodium chloride, to give a crystalline precipitate. The precipitate was collected by filtration, washed successively with two portions of water and one portion of acetone, and dried under reduced pressure to give 340 mg of the desired compound as a pale brown crystalline powder, yield 12.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180836
Source datasetuspto-grants-1993_01
ORD IDord-1efdea2e08cc4d0caed8c860df74acbc
Source noteuspto-grants-1993_01