Quinoline → 2-Decen-1-ol, (Z)-

HRID 1858885

Reaktionsgleichung

Reaktionsgleichung von HRID 1858885
[CH2:1]([OH:11])[C:2]#[C:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].N1C2C(=CC=CC=2)C=CC=1>[Pd].CC([O-])=O.CC([O-])=O.[Pb+2].[Pd]>[CH2:1]([OH:11])/[CH:2]=[CH:3]\[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Komponenten

5

Versuchsvorschrift

To a solution of 10.0 g of 2-decyn-1-ol in 150 ml of petroleum ether was added 500 mg of Pd on CaCO3 poisoned with lead (Lindlar catalyst). Quinoline (2.0 ml) was then added to this mixture and the flask was evacuated (house vacuum, ca. 50 mm Hg) and flushed with H2 three times and left under a H2 atmosphere. The mixture was stirred vigorously until uptake of H2 was no longer evident and TLC (SiO2 /20% ether:pet. ether) showed no starting material. The catalyst was removed by filtration through a 4 cm pad of celite and the filtrate was washed two times with 100 ml of 1 N HCl, once with 100 ml of saturated NaHCO3, once with 100 ml of brine, dried over MgSO4, filtered and the solvent evaporated to give a pale yellow oil. Kugelrohr distillation (100-120° C. oven, 0.2 mm) affords 8.81 g of clear oil. 1H NMR δ 5.57 (m,2), 4.20 (t, 2, J=5 Hz), 2.07 (dd, 2, J=6, 12 Hz), 1.5-1.1 (m, 10), 0.88 (t, 3, J=7 Hz).

Aufarbeitung

  1. customthe flask was evacuated (house vacuum, ca. 50 mm Hg)
  2. customflushed with H2 three times
  3. waitleft under a H2 atmosphere
  4. customThe catalyst was removed by filtration through a 4 cm pad of celite
  5. washthe filtrate was washed two times with 100 ml of 1 N HCl
  6. dry with materialonce with 100 ml of saturated NaHCO3, once with 100 ml of brine, dried over MgSO4
  7. filtrationfiltered
  8. customthe solvent evaporated
  9. customto give a pale yellow oil
  10. distillationKugelrohr distillation (100-120° C. oven, 0.2 mm)

Quellen und Nachweise

ORD-Eintrag
ord-fe0519af63964a8e8c29fd940badcc4b
Quelldatensatz
uspto-grants-2000_11
Patentnummer
US06153589

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