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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030794Generated: November 4, 2026

m-Chloroperbenzoic acid → 2-(2-Dimethylaminobenzylsulfinyl)-3-methylquinoxaline

https://huagongshe.com/reaction/1030794

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 19820959HCID 19820959—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product2-(2-Dimethylaminobenzylsulfinyl)-3-methylquinoxalineHCID 1405218231.3%

Reaction Steps

In a mixture of 10 ml of chloroform and 10 ml of methanol was dissolved 1.73 g of 2-(2-dimethylaminobenzylthio)-3-methylquinoxaline hydrochloride. To the chilled solution kept at a temperature of lower than 0° C. (temperature of solution) was portionwise added 1.14 g of m-chloroperbenzoic acid (purity: 80%). After the reaction was complete, chloroform and saturated aqueous NaHCO3 solution were added to the reaction mixture. The organic layer was separated and dried over sodium sulfate. The sodium sulfate was then removed by filtration, and the solvent was evaporated under reduced pressure from the filtrate. The residue was purified by silica gel column chromatography (chloroform/methanol), and recrystallized from ethyl acetate/hexane to give 0.51 g of 2-(2-dimethylaminobenzylsulfinyl)-3-methylquinoxaline as a pale brown crystalline powder, m.p. 68°-70° C. (decompn.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106976
Source datasetuspto-grants-1992_04
ORD IDord-1d0db769d9c24b9dab42ca65ee1904c7
Source noteuspto-grants-1992_04