Tetrabutylammonium Fluoride → (S)-5-Phenylpent-1-yn-3-ol
反応式
[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]=1参加物
実験手順
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%).
後処理
- 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)
出典と根拠
- ORDレコード
- ord-b6d2b76bd6ce4bd89dc90191eeb12939
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09242954B2
反応ノート
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