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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071531Generated: November 4, 2026

m-Chloroperbenzoic acid → 2-[(1H-Benzimidazole-2-sulfinyl)methyl]aniline

https://huagongshe.com/reaction/1071531

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantBenzenamine, 2-[(1H-benzimidazol-2-ylthio)methyl]-HCID 11054238—
SolventChloroformHCID 6212—
Product2-[(1H-Benzimidazole-2-sulfinyl)methyl]anilineHCID 1353747962.4%

Reaction Conditions

Temperature-10 °C

Reaction Steps

The title product of Example 2 (830 mg, 3.25 mmole) was dissolved in about 200 ml of boiling chloroform and then cooled to about −10° C. A solution of 662 mg (ca. 3.25 mmole) of ca. 85% m-chloroperoxybenzoic acid in 10 ml of chloroform was then added with stirring over about ten minutes. After another thirty minutes, the reaction was quenched with 4 drops of dimethylsulfide and a white solid was collected by filtration. The solid was washed sequentially with chloroform and diethyl ether, then air dried, giving 550 mg of the title compound: m.p. 164-165° C. Analysis. Calc'd. for C14H13N3OS*½ H2O: C,59.98; H,5.03; N, 15.00; S, 11.44. Found: C, 60.11; H, 4.82; N, 14.93; S, 11.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906078B2
Source datasetuspto-grants-2005_06
ORD IDord-881daf4f26d649af8ce527c8e4139322
Source noteuspto-grants-2005_06