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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1588714Erstellt: 26. Oktober 2026

Tetrabutylammonium Fluoride → alpha-Ethynylbenzenemethanol

https://huagongshe.com/reaction/1588714

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrabutylammonium FluorideHCID 2724141—
Edukt1-Phenyl-3-(trimethylsilyl)-2-propyn-1-olHCID 2760416—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-EthynylbenzenemethanolHCID 2015581,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Place a mixture of α-[(trimethylsilyl)ethynyl]-benzene-methanol (4.09 g, 20 mmol) and tetrahydrofuran (25 mL) under argon atmosphere and cool to 0° C. Add, by dropwise addition, tetra-n-butylammonium fluoride (25 mL of a 1M solution in tetrahydrofuran, 25 mmol). Allow to warm to room temperature and stir for 1 hour. Partition between ethyl ether and water. Separate the organic phase, wash with saturated aqueous sodium chloride and concentrate in vacuo. Purify by silica gel chromatography (15% ethyl acetate/hexane) then purify further by distillation to yield 2.15 g of the title compound; bp 100°-110° C. @0.1 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05223518
Quelldatensatzuspto-grants-1993_06
ORD IDord-3a223550e8214c68a932503169f4d82d
Quellennotizuspto-grants-1993_06