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HRID 593405作成日:2026年10月27日

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

https://huagongshe.com/reaction/593405

反応式

関与物質

役割名称HCID仕込み量
反応物(Triisopropylsilyl)acetyleneHCID 2734682—
反応物N-methoxy-N-methyl-3-phenylpropanamideHCID 3785569—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物5-Phenyl-1-(triisopropylsilyl)pent-1-yn-3-oneHCID 90032254—

反応条件

温度0 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242954B2
出典データセットuspto-grants-2016_01
ORD IDord-af10c029f4c84a9493c7ea9dbc2ef903
出典メモuspto-grants-2016_01