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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418243Generated: October 25, 2026

m-Chloroperbenzoic acid → HCID 10021071, compound

https://huagongshe.com/reaction/2418243

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-trifluoromethyl-2-[(4-methoxy-2-pyridylmethyl)thio]-(1H)-benzimidazoleHCID 10020071—
SolventDichloromethaneHCID 6344—
ProductHCID 10021071HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04472409
Source datasetuspto-grants-1984_09
ORD IDord-ac2e7237c81246a6ac20aa78dcce5ef7
Source noteuspto-grants-1984_09