HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603284Generated: October 25, 2026
Hexane → 1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanone
https://huagongshe.com/reaction/1603284
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1-Fluoro-2,4,6-trimethylpyridinium Trifluoromethanesulfonate [Fluorinating Reagent] | HCID 2724575 | — |
| Reactant | 1-(2,4-Difluorophenyl)-2-(methylsulfanyl)ethan-1-one | HCID 10655717 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanone | HCID 10632701 | 90.8% |
Reaction Steps
To a 20 ml solution of 0.5 g (2.5 mmol) of 2',4'-difluoro-2-(methylthio)acetophenone [Compound (2a-1)] in 1,2-dichloroethane, 1.1 g (3.8 mmol) of N-fluoro-2,4,6-trimethylpyridinium triflate ("Onoda Florinate FP-T300", trade name; product of Chichibu Onoda Co., Ltd.) were added at room temperature, followed by stirring at the same temperature for 12 hours. The reaction mixture was added to n-hexane. The insoluble matter so precipitated was filtered off. The insoluble matter was then washed with ethyl ether, followed by combination with the hexane layer. The layers so combined were washed successively with water and saturated saline, followed by drying over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure, whereby 0.50 g of the title Compound (2b-1) was obtained in the form of a light yellow oil (yield: 91.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05986144 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-ab5ec0f149d14569bb46c3ee35dcdcbf |
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| Source note | uspto-grants-1999_11 |
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