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HRID 2058作成日:2026年10月26日

Acetylene → 2-Phenylbut-3-yn-1-ol

https://huagongshe.com/reaction/2058

反応式

関与物質

役割名称HCID仕込み量
反応物AcetyleneHCID 6326—
反応物2-Phenyl-4-trimethylsilyl-but-3-yn-1-olHCID 14140996—
触媒Silver NitrateHCID 24470—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物2-Phenylbut-3-yn-1-olHCID 2255935095.8%

反応条件

温度-5 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728695
出典データセットuspto-grants-1998_03
ORD IDord-5b0feb349090451da9847168db764b49
出典メモuspto-grants-1998_03