HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418243Generated: October 25, 2026
m-Chloroperbenzoic acid → HCID 10021071, compound
https://huagongshe.com/reaction/2418243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4-trifluoromethyl-2-[(4-methoxy-2-pyridylmethyl)thio]-(1H)-benzimidazole | HCID 10020071 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10021071 | HCID 10021071 | — |
Reaction Steps
2.3 g of commercially available 85% strength m-chloroperoxybenzoic acid, dissolved in 30 ml of methylene chloride, are added dropwise to a solution, cooled to -30° C., of 3.0 g (0.0088 mole) of 4-trifluoromethyl-2-[(4-methoxy-2-pyridylmethyl)thio]-(1H)-benzimidazole in 50 ml of methylene chloride over the course of 45 minutes. The resulting mixture is then stirred for a further 60 minutes, and the temperature is subsequently allowed to rise to 0° C. After the mixture is washed with saturated aqueous sodium carbonate solution (30 ml), it is dried over sodium sulfate, and the solvent is stripped off in vacuo. The solid residue which remains is recrystallized successively from isopropanol and acetonitrile. Yield: 1.6 g of title compound, m.p. 150° to 151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04472409 |
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| Source dataset | uspto-grants-1984_09 |
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| ORD ID | ord-ac2e7237c81246a6ac20aa78dcce5ef7 |
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| Source note | uspto-grants-1984_09 |
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