Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736160Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 10769055, compound

https://huagongshe.com/reaction/1736160

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 10649631HCID 10649631—
ReactantSodium BisulfiteHCID 23665763—
SolventDichloromethaneHCID 6344—
ProductHCID 10769055HCID 1076905594%

Reaction Steps

203 mg (0.391mmol) of 6,8-difluoro-2-(3-fluoro-4-pivaloylaminophenyl)-7-methylthio-5-pivaloylamino-4H-1-benzopyran-4-one obtained in Example 85 (2) was dissolved in 5 mL of dichloromethane, 850 mg (3.91 mmol) of m-chloroperbenzoic acid was added under ice-cooling and the mixture was stirred at room temperature for 3 hours. An aqueous solution of sodium hydrogensulfite was added to the reaction solution and the mixture was extracted once with chloroform. The organic layer was washed once with an aqueous solution of sodium bicarbonate, once with water and once with an aqueous saturated solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (chloroform:ethyl acetate=40:l) to give 204 mg of 6,8-difluoro-2-(3-fluoro-4-pivaloylaminophenyl)-7-methylsulfonyl-5-pivaloylamino-4H-1-benzopyran-4-one (yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05539112
Source datasetuspto-grants-1996_07
ORD IDord-1b021e9b67fa467198c2fdbd13cc62d9
Source noteuspto-grants-1996_07