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HRID 593405생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/593405

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참여 물질

역할이름HCID투입량
반응물(Triisopropylsilyl)acetyleneHCID 2734682—
반응물N-methoxy-N-methyl-3-phenylpropanamideHCID 3785569—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물5-Phenyl-1-(triisopropylsilyl)pent-1-yn-3-oneHCID 90032254—

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온도0 °C

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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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09242954B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-af10c029f4c84a9493c7ea9dbc2ef903
출처 메모uspto-grants-2016_01