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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413753Generated: October 28, 2026

m-Chloroperbenzoic acid → HCID 178510674, compound

https://huagongshe.com/reaction/413753

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178510673HCID 178510673—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178510674HCID 178510674—

Reaction Steps

To a solution of 15 g (35.5 mmol) of 1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoromethylsulfenyl-5-hydroxypyrazole in 125 ml of dichloromethane at room temperature was added a solution of m-chloroperbenzoic acid (8.76 g, 70%, 35.5 mmol) in 375 ml of dichloromehane. The resulting solution was stirred at room temperature for 17 hr. It was then concentrated and triturated with ethyl acetate and heptane (1:2). Upon filtration a solid was obtained. This solid was dissolved in ethyl acetate and stirred with saturated sodium bicarbonate solution. Ther layers were separated and the aqueous layer was extracted with three times of ethyl acetate. The combined organic layer was dried (magnesium sulfate) and concentrated. Upon chromatographic purification via silica gel column, a solid (5.7 g, 13.01 mol, 37%) was obtained as the desired product, mp 185-187d.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06569886B2
Source datasetuspto-grants-2003_05
ORD IDord-41c10ab3329b4462ae795345331293ca
Source noteuspto-grants-2003_05