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HRID 2372431作成日:2026年10月27日

Sodium Chloride → 1,1-Bis(methylthio)-2-(4-phenoxyphenyl)-1 butene

https://huagongshe.com/reaction/2372431

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ChlorideHCID 5234—
反応物HexaneHCID 8058—
反応物3-Phenoxy-1-phenylpropan-1-oneHCID 3876355—
反応物Bis(methylthio)(trimethylsilyl)methaneHCID 11008541—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1,1-Bis(methylthio)-2-(4-phenoxyphenyl)-1 buteneHCID 1467413396.2%

反応条件

温度-73 °C

反応手順

Trimethylsilyl-bis(methylthio)methane, 2.65 g, was dissolved in 15 ml of tetrahydrofuran and 7 ml of 1.6 mole hexane solution of n-butyl lithium was dropwise added to the solution in an argon flow under ice cooling. The mixture was stirred at the same temperature for 30 minutes. After cooling to -73° C., a solution of 2.26 g of 4-phenoxypropiophenone in 5 ml of tetrahydrofuran was dropwise added to the mixture. Then, the temperature was gradually elevated to room temperature followed by stirring for 16 hours. After saturated sodium chloride aqueous solution was added to the mixture, it was extracted with chloroform. After drying the chloroform phase over magnesium sulfate, the solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (chloroform : hexane =1 : 1) to give 3.04 g of the oily product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05098928
出典データセットuspto-grants-1992_03
ORD IDord-3ff5bc31306346dca8e5fcacd697f3f3
出典メモuspto-grants-1992_03