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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598513Generated: October 30, 2026

Trifluoroiodomethane → 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-(trifluoromethylsulfenyl)pyrazole

https://huagongshe.com/reaction/1598513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroiodomethaneHCID 16843—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178481742HCID 178481742—
SolventTetrahydrofuranHCID 8028—
Product3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-(trifluoromethylsulfenyl)pyrazoleHCID 18929421—

Reaction Steps

To a suspension of 0.13 g of 60% oily sodium hydride in 10 ml of anhydrous tetrahydrofuran was added dropwise 0.7 g of 3-(2,6-dichloro-4-trifluoromethylphenyl)-1-methyl-5-mercaptopyrazole (2) in 2.0 ml of anhydrous tetrahydrofuran at 0° C., and the mixture was stirred at room temperature for 1 hour. Subsequently, with addition of an excess of trifluoromethyl iodide, the mixture was stirred for 4 hours as contained in a sealed container. Ice water was added to the reaction mixture, the mixture was thereafter extracted with ethyl acetate, and the extracts were combined together, washed with brine and dried over magnesium sulfate. The solvent was distilled off under reduced pressure to obtain a residue, which was then purified by column chromatography on silica gel (eluent: ethyl acetate/hexane=1/5), giving 0.6 g of the desired compound in the form of a colorless oil (yield 48.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739083
Source datasetuspto-grants-1998_04
ORD IDord-6c106ea71a5b4e4abcfc7529820edce0
Source noteuspto-grants-1998_04