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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598514Generated: November 2, 2026

m-Chloroperbenzoic acid → 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfinylpyrazole

https://huagongshe.com/reaction/1598514

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazoleHCID 18929419—
SolventChloroformHCID 6212—
Product3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfinylpyrazoleHCID 18929401—

Reaction Steps

A 0.3 g quantity of 70% m-chloroperbenzoic acid was slowly added to 0.3 g of 3-(2,6-dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazole (compound 1) in 20 ml of anhydrous chloroform at room temperature with stirring, followed by stirring for 3 hours. The reaction mixture was poured into a saturated aqueous solution of sodium hydrogencarbonate, an organic layer was then separated off, washed with 5% aqueous sodium hydroxide solution and with brine and dried over anhydrous magnesium sulfate. The solvent was thereafter distilled off under reduced pressure, giving 0.3 g of the desired compound in the form of white crystals (quantitative crude yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739083
Source datasetuspto-grants-1998_04
ORD IDord-e03c7faaf81e4a7a84f8aef0f783f330
Source noteuspto-grants-1998_04