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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586466Generated: November 2, 2026

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

https://huagongshe.com/reaction/1586466

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 mMol) was dissolved in about 200 ml of boiling chloroform and then cooled to about -10° C. A solution of 662 mg (ca. 3.25 mmol) 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. Anal. Calc'd. for C14H13N3OS*1/2 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 numberUS05945425
Source datasetuspto-grants-1999_08
ORD IDord-bb492e525baa4d3bb4b683f4d53a5e03
Source noteuspto-grants-1999_08