참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Chloride | HCID 5234 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | 3-Phenoxy-1-phenylpropan-1-one | HCID 3876355 | — |
| 반응물 | Bis(methylthio)(trimethylsilyl)methane | HCID 11008541 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1,1-Bis(methylthio)-2-(4-phenoxyphenyl)-1 butene | HCID 14674133 | 96.2% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05098928 |
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| 출처 데이터셋 | uspto-grants-1992_03 |
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| ORD ID | ord-3ff5bc31306346dca8e5fcacd697f3f3 |
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| 출처 메모 | uspto-grants-1992_03 |
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