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HRID 2058生成日期:2026年10月23日

乙炔 → 2-苯基丁-3-炔-1-醇

https://huagongshe.com/zh-CN/reaction/2058

反应方程式

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-olHCID 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 2255935095.8%

反应条件

温度-5 °C

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

DOI10.6084/m9.figshare.5104873.v1
专利号US05728695
来源数据集uspto-grants-1998_03
ORD IDord-5b0feb349090451da9847168db764b49
来源说明uspto-grants-1998_03