Potassium Hydroxide → (S)-5-Phenyl-1-(triisopropylsilyl)pent-1-yn-3-ol

HRID 593406Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 593406
[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

Komponenten

5

Versuchsvorschrift

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)).

Aufarbeitung

  1. concentrationThe mixture was concentrated in vacuo
  2. customto give the crude product
  3. customThis was purified by column chromatography on silica
  4. washeluting with petrol/Et2O (20:1 to 10:1)

Quellen und Nachweise

ORD-Eintrag
ord-7d3f6702dcec485a92774ca78c2186ad
Quelldatensatz
uspto-grants-2016_01
Patentnummer
US09242954B2

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