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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2058Erstellt: 25. Oktober 2026

Acetylene → 2-Phenylbut-3-yn-1-ol

https://huagongshe.com/reaction/2058

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyleneHCID 6326—
Edukt2-Phenyl-4-trimethylsilyl-but-3-yn-1-olHCID 14140996—
KatalysatorSilver NitrateHCID 24470—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt2-Phenylbut-3-yn-1-olHCID 2255935095,8%

Reaktionsbedingungen

Temperatur-5 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728695
Quelldatensatzuspto-grants-1998_03
ORD IDord-5b0feb349090451da9847168db764b49
Quellennotizuspto-grants-1998_03