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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1603285Erstellt: 25. Oktober 2026

Chloroform → 2-Methylthio-2,2,2',4'-tetrafluoroacetophenone

https://huagongshe.com/reaction/1603285

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktHexaneHCID 8058—
EduktN-Fluoro-4-methylpyridinium-2-sulfonateHCID 2737404—
Edukt1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanoneHCID 10632701—
Lösungsmittel1,1,2-TrichloroethaneHCID 6574—
Produkt2-Methylthio-2,2,2',4'-tetrafluoroacetophenoneHCID 1022034747,5%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

In a 20 ml solution of 0.5 g (2.3 mmol) of 2-methylthio-2,2',4'-trifluoroacetophenone [Compound (2b-1)] in 1,1,2-trichloroethane, 0.7 g (3.7 mmol) of N-fluoro-4-methylpyridinium-2-sulfonate ("MEC-02", trade name; Daikin Industries, Ltd.) was added at an internal temperature of 80° C., followed by stirring at an internal temperature of 100° C. for 20 minutes. After cooling, 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. The residue so obtained was subjected to chromatography on a silica gel column using chloroform, whereby 0.26 g of the title Compound (2c-1) was obtained in the form of a light yellow oil (yield: 48.1%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05986144
Quelldatensatzuspto-grants-1999_11
ORD IDord-9ff763c582c047de971aa0222fe2b9e3
Quellennotizuspto-grants-1999_11