Potassium Hydroxide → (S)-5-Phenyl-1-(triisopropylsilyl)pent-1-yn-3-ol
反応式
[OH-].[K+].[C:3]1([CH2:9][CH2:10][C:11](=[O:24])[C:12]#[C:13][Si:14]([CH:21]([CH3:23])[CH3:22])([CH:18]([CH3:20])[CH3:19])[CH:15]([CH3:17])[CH3:16])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>CC1C=CC(C(C)C)=CC=1.CC1C=CC(S([N-][C@H]([C@@H](N)C2C=CC=CC=2)C2C=CC=CC=2)(=O)=O)=CC=1.Cl[Ru+].C(O)CC>[C:3]1([CH2:9][CH2:10][C@H:11]([OH:24])[C:12]#[C:13][Si:14]([CH:18]([CH3:20])[CH3:19])([CH:15]([CH3:17])[CH3:16])[CH:21]([CH3:22])[CH3:23])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1参加物
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
Following a modified procedure of Trost (Trost, B. M. et al., J. Am. Chem. Soc. 128, 6745-6754 (2006)); Potassium hydroxide (8.5 mg, 0.15 mmol, 1.2 mol %) and RuCl(p-cymene)[(S,S)-Ts-DPEN] (80.7 mg, 0.127 mmol, 1 mol %) were added to) PrOH (110 ml) and the resultant mixture was stirred for 2 min at r.t. 5-Phenyl-1-(triisopropylsilyl)pent-1-yn-3-one 84 (4.0 g, 12.7 mmol, 1 eq.) was added via syringe and the mixture was stirred at r.t. for 45 min. The mixture was concentrated in vacuo to give the crude product. This was purified by column chromatography on silica, eluting with petrol/Et2O (20:1 to 10:1), giving the title product 85 as a clear, colourless oil (4.0 g, 99%). The enantiomeric excess was determined to be 99% via HPLC analysis of its derivative 87. Analytical data consistent with the literature (Trost, B. M. et al., J. Am. Chem. Soc. 128, 6745-6754 (2006)).
後処理
- concentrationThe mixture was concentrated in vacuo
- customto give the crude product
- customThis was purified by column chromatography on silica
- washeluting with petrol/Et2O (20:1 to 10:1)
出典と根拠
- ORDレコード
- ord-7d3f6702dcec485a92774ca78c2186ad
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09242954B2
反応ノート
読み込み中…