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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612042Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 178510674, compound

https://huagongshe.com/reaction/1612042

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 dichloromethane. 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. The layers were separated and the aqueous layer was extracted three times with 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 numberUS06992099B2
Source datasetuspto-grants-2006_01
ORD IDord-a3b98d8c86324498bbd0b1a638dea6f8
Source noteuspto-grants-2006_01