HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049280Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 20345013, compound
https://huagongshe.com/reaction/2049280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 13373882 | HCID 13373882 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20345013 | HCID 20345013 | 71.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04197307 |
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| Source dataset | uspto-grants-1980_04 |
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| ORD ID | ord-2741aee8e9d74ff7af14e459169ab909 |
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| Source note | uspto-grants-1980_04 |
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