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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598515Generated: November 2, 2026

Sodium Sulfite → 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfonylpyrazole

https://huagongshe.com/reaction/1598515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfinylpyrazoleHCID 18929401—
Reactant3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazoleHCID 18929419—
SolventChloroformHCID 6212—
Product3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfonylpyrazoleHCID 18929424—

Reaction Steps

A 0.3 g quantity of 70% m-chloroperbenzoic acid was slowly added to 0.2 g of 3-(2,6-dichloro-4-trifluoromethylphenyl)-1-methyl-5-methylsulfenylpyrazole (compound 6) in 20 ml of anhydrous chloroform at room temperature with stirring, followed by further stirring overnight. The reaction mixture was poured into a 10% aqueous sodium sulfite solution, 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-98a0b3bab57c4faf8f1f3a06795f6f04
Source noteuspto-grants-1998_04