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HRID 1586434作成日:2026年10月27日

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

https://huagongshe.com/reaction/1586434

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物HexaneHCID 8058—
反応物Pyridinium, 1-fluoro-, 1,1,1-trifluoromethanesulfonate (1:1)HCID 2724576—
反応物1-(2,4-Difluorophenyl)-2-(methylsulfanyl)ethan-1-oneHCID 10655717—
溶媒1,1,2-TrichloroethaneHCID 6574—
生成物2-Methylthio-2,2,2',4'-tetrafluoroacetophenoneHCID 1022034747%

反応条件

温度100 °C

反応手順

To a 20 ml solution of 0.5 g (2.5 mmol) of 2',4'-difluoro-2-(methylthio)acetophenone [Compound (2a-1)] in 1,1,2-trichloroethane, 3.0 g (12.1 mmol) of N-fluoropyridinium triflate ("Onoda Fluorinate FP-T500", trade name; product of Chichibu Onoda Co., Ltd.) were added at an internal temperature of 80° C., followed by stirring at an internal temperature of 100° C. for one hour. After cooling, the reaction mixture was added to n-hexane. The insoluble matter 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 distilled off under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column using chloroform, whereby 0.28 g of the title Compound (2c-1) was obtained in the form of a light yellow oil (yield: 47.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05945438
出典データセットuspto-grants-1999_08
ORD IDord-7ee50cf0d8fe4cadba3e9d4c1d1dd879
出典メモuspto-grants-1999_08