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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621543Generated: November 2, 2026

m-Chloroperbenzoic acid → 2-((1H-Benzimidazol-2-ylsulfinyl)methyl)-N,N-dimethylbenzenamine

https://huagongshe.com/reaction/621543

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantBenzenamine, 2-[(1H-benzimidazol-2-ylthio)methyl]-N,N-dimethyl-HCID 10265859—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product2-((1H-Benzimidazol-2-ylsulfinyl)methyl)-N,N-dimethylbenzenamineHCID 11915758.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(2-Dimethylaminobenzylthio)benzimidazole (4.8 g) was dissolved in a mixture of 40 ml of chloroform and 5 ml of methanol. After the solution was chilled to 0° C., 3.86 g of m-chloroperbenzoic acid (purity: 70%) was added portionwise. Ten minutes later, a saturated aqueous NaHCO3 solution was added to the reaction mixture, and the resulting mixture was extracted with chloroform. The chloroform solution was washed with saturated brine and then dried over anhydrous sodium sulfate. The chloroform was distilled off under reduced pressure and the residue was recrystallized from a mixture of chloroform and ether to obtain 2.97 g of 2-(2-dimethylaminobenzylsulfinyl)benzimidazole as a colorless crystalline product (m.p. 112° C., decomposed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824856
Source datasetuspto-grants-1989_04
ORD IDord-53a827f9d1eb4b3ca943ba97c48d6248
Source noteuspto-grants-1989_04