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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroiodomethane | HCID 16843 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178481742 | HCID 178481742 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2,6-Dichloro-4-trifluoromethylphenyl)-1-methyl-5-(trifluoromethylsulfenyl)pyrazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05739083 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-6c106ea71a5b4e4abcfc7529820edce0 |
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| Source note | uspto-grants-1998_04 |
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