関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Chloride | HCID 5234 | — |
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | 3-Phenoxy-1-phenylpropan-1-one | HCID 3876355 | — |
| 反応物 | Bis(methylthio)(trimethylsilyl)methane | HCID 11008541 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,1-Bis(methylthio)-2-(4-phenoxyphenyl)-1 butene | HCID 14674133 | 96.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05098928 |
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| 出典データセット | uspto-grants-1992_03 |
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| ORD ID | ord-3ff5bc31306346dca8e5fcacd697f3f3 |
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| 出典メモ | uspto-grants-1992_03 |
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