Tetrabutylammonium Fluoride → (S)-5-Phenylpent-1-yn-3-ol
반응식
[F-].C([N+](CCCC)(CCCC)CCCC)CCC.[C:19]1([CH2:25][CH2:26][C@H:27]([OH:40])[C:28]#[C:29][Si](C(C)C)(C(C)C)C(C)C)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C1COCC1>[C:19]1([CH2:25][CH2:26][C@H:27]([OH:40])[C:28]#[CH:29])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1참가 물질
실험 절차
Following a modified procedure of Trost (Trost, B. M. et al., J. Am. Chem. Soc. 128, 6745-6754 (2006)); Tetrabutylammonium fluoride (1.0 M in THF, 25 ml, 25 mmol, 2.5 eq.) was added to a solution of (S)-5-phenyl-1-(triisopropylsilyl)pent-1-yn-3-ol 85 (3.165 g, 10 mmol, 1 eq.) in THF (95 ml). The reaction mixture was stirred for 1 h at r.t. and then quenched by addition of saturated aq. NH4Cl (50 ml). The mixture was extracted with Et2O (3×40 ml), 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 (10:1 to 9:1), giving the title product 86 as a clear, colourless oil (1.6 g, 99%).
후처리
- customquenched by addition of saturated aq. NH4Cl (50 ml)
- extractionThe mixture was extracted with Et2O (3×40 ml)
- washthe combined organic phases were washed with brine (50 ml)
- dry with materialbefore being dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customto give the crude product
- customThis was purified by column chromatography on silica
- washeluting with petrol/Et2O (10:1 to 9:1)
출처 및 근거
- ORD 기록
- ord-b6d2b76bd6ce4bd89dc90191eeb12939
- 출처 데이터셋
- uspto-grants-2016_01
- 특허 번호
- US09242954B2
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