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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593405Erstellt: 25. Oktober 2026

(Triisopropylsilyl)acetylene → 5-Phenyl-1-(triisopropylsilyl)pent-1-yn-3-one

https://huagongshe.com/reaction/593405

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(Triisopropylsilyl)acetyleneHCID 2734682—
EduktN-methoxy-N-methyl-3-phenylpropanamideHCID 3785569—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Phenyl-1-(triisopropylsilyl)pent-1-yn-3-oneHCID 90032254—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Following a procedure of Trost (Trost, B. M. et al., J. Am. Chem. Soc. 128, 6745-6754 (2006)); n-Butyllithium (2.5 M in hexanes, 10.4 ml, 26 mmol, 1.7 eq.) was added dropwise to a solution of triisopropylsilyl acetylene (5.8 ml, 26 mmol, 1.7 eq.) in THF (53 ml) at −78° C. After addition, the mixture was allowed to warm slowly to 0° C. and stirred for 1 h. The mixture was cooled to −78° C. and a solution of 83 (3.0 g, 15.3 mmol, 1 eq.) in THF (20 ml) was added dropwise. The mixture was then allowed to slowly warm to −10° C. and stirred for 1 h before being quenched by the addition of saturated aq. NH4Cl (50 ml). The mixture was extracted with EtOAc (3×30 ml) and the combined organic phases were washed with brine (50 ml) before being dried (MgSO4), filtered and concentrated to give the crude product. This was purified by column chromatography on silica, eluting with petrol/Et2O (100:0 to 98:2), giving the title product 84 as a clear, colourless oil (4.61 g, 96%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242954B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-af10c029f4c84a9493c7ea9dbc2ef903
Quellennotizuspto-grants-2016_01