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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030795Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 14052183, compound

https://huagongshe.com/reaction/1030795

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 14052178HCID 14052178—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 14052183HCID 1405218328.8%

Reaction Steps

In a mixture of 35 ml of chloroform and 3 ml of methanol was dissolved 3.71 g of 2-(2-dimethylaminobenzylthio)-3,6,7-trimethylquinoxaline. To the chilled solution kept at a temperature of lower than 0° C. (temperature of solution) was slowly added 2.45 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 (acetone/hexane). The eluate was concentrated and the resulting residue was crystallized from ether/hexane to give 1.12 g of 2-(2-dimethylaminobenzylsulfinyl)-3,6,7-trimethylquinoxaline as a yellow crystalline powder, m.p. 83°-88° C. (decompn.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106976
Source datasetuspto-grants-1992_04
ORD IDord-053616ead30442099effa9060af69fa8
Source noteuspto-grants-1992_04