参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 乙炔 | HCID 6326 | — |
| 反应物 | 2-Phenyl-4-trimethylsilyl-but-3-yn-1-ol | HCID 14140996 | — |
| 催化剂 | 硝酸银 | HCID 24470 | — |
| 溶剂 | 乙醇 | HCID 702 | — |
| 溶剂 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 产物 | 2-苯基丁-3-炔-1-醇 | HCID 22559350 | 95.8% |
反应步骤
2-Phenyl-4-trimethylsilyl-but-3-yn-1-ol (Chem. Ber. (1988), 121, 1315-1320) (7.8 g) was dissolved in ethanol and the solution was cooled to -5° C. A solution of silver nitrate (8.9 g) in ethanol (60 ml) and water (21 ml) was added dropwise to the acetylene solution such that the temperature remained below 5° C. This precipitated the acetylene as the silver complex. A solution of potassium cyanide (17 g) in water (30 ml) was added dropwise to the stirred acetylene mixture and the resulting mixture was stirred at room temperature for 30 minutes. The mixture mainly dissolved and was diluted with water and extracted with ethyl acetate. The organic extracts were washed with brine, dried (MgSO4) and evaporated. The residue was purified on silica using 10% ethyl acetate in hexane as eluant to afford the title compound (5 g) as a colourless oil.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US05728695 |
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| 来源数据集 | uspto-grants-1998_03 |
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| ORD ID | ord-5b0feb349090451da9847168db764b49 |
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| 来源说明 | uspto-grants-1998_03 |
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