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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049280Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 20345013, compound

https://huagongshe.com/reaction/2049280

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 13373882HCID 13373882—
ReactantSodium BisulfiteHCID 23665763—
SolventChloroformHCID 6212—
ProductHCID 20345013HCID 2034501371.1%

Reaction Steps

A solution of 19.5 g of 90% pure m-chloroperbenzoic acid in 450 ml of chloroform is added dropwise in the course of 30 minutes to a solution, which has been cooled to 0° to 5° C., of 35 g of 5-chloro-6-(2',4'-dichlorophenoxy)-2-methylthio-benzimidazole in 1,750 ml of chloroform, with stirring. The mixture is stirred for a further 3 hours at 0° to 5° C. and then for 15 hours at room temperature and then is freed from the small amount of precipitate which arises. The filtrate, which still contains residues of m-chloroperbenzoic acid, is treated with sodium bisulphite solution, washed with water, dried over calcium chloride, filtered and concentrated in vacuo. After recrystallising the residue from 500 ml of ethyl acetate, and at the same time clarifying the hot solution with active charcoal, and then drying the white crystals at 50° C., 26 g of 5-chloro-6-(2',4'-dichlorophenoxy)-2-methylsulphinyl-benzimidazole with a melting point of 206°-208° C. are obtained, which corresponds to a yield of 69%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04197307
Source datasetuspto-grants-1980_04
ORD IDord-2741aee8e9d74ff7af14e459169ab909
Source noteuspto-grants-1980_04