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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601402Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 44329885, compound

https://huagongshe.com/reaction/1601402

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 21831301HCID 21831301—
SolventDichloromethaneHCID 6344—
ProductHCID 44329885HCID 4432988535.6%

Reaction Steps

In 3 ml of methylene chloride was dissolved 80 mg of 6-cyano-2,2-bisfluoromethyl-4-(2-pyridyl)-2H-1-benzopyran and 75.7 mg of m-chloroperbenzoic acid (70%) was added thereto with stirring under ice-cooling. The mixture was stirred at room temperature for 15 hours. After addition of 28 mg of m-chloroperbenzoic acid (70%), the mixture was further stirred for 19 hours. Sodium bicarbonate solution was added thereto and the mixture was extracted with methylene chloride. After the organic layer was washed with water and dried, the solvent was distilled off. The resultant residue was purified using silica gel column chromatography (developing solution, MeOH:CH2Cl2 =1:99) to obtain 30 mg of 2-(6-cyano-2,2-bisfluoromethyl-2H-1-benzopyran-4-yl)pyridine N-oxide represented by the following formula having a melting point of 204-207° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977167
Source datasetuspto-grants-1999_11
ORD IDord-6b3cdd1bb18349f885380339c7237f66
Source noteuspto-grants-1999_11