Реакция #2146736

ord-f0c7fd6f53dd429eacba6619bfac7fb3

Уравнение реакции

c1ccc2ncccc2c1
quinoline
CCC/C=C\CC(C)CC(O)C#CC(C)(C)O
(9Z)-2,7-dimethyltridec-9-en-3-yne-2,5-diol
CCC/C=C\CC(C)CC(O)/C=C\C(C)(C)O
(3Z,9Z)-2,7-dimethyltrideca-3,9-diene-2,5-diol
Выход 55.1%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe flask was evacuated
  2. 2
    Другоеflushed with nitrogen three times, and three times
  3. 3
    Другоеevacuated
  4. 4
    Другоеflushed with hydrogen
  5. 5
    ДругоеThe resulting reaction mixture
  6. 6
    Фильтрацияthe catalyst filtered off by suction over a pad of Celite
  7. 7
    ДругоеAfter removal of the solvent
  8. 8
    Другоеin a rotary evaporator under reduced pressure
  9. 9
    Другоеthe resulting crude product (8.07 g) was purified by flash chromatography (100 g of silica gel, pentane/ether, 1:1, Rf=0.28)

Методика

At room temp., 520 mg (0.488 mmol) of 10% palladium on barium sulphate and 190 mg (1.47 mmol) of quinoline were added to a stirred solution of 7.70 g (32.3 mmol) of this (9Z)-2,7-dimethyltridec-9-en-3-yne-2,5-diol in 170 mL of ethanol. The flask was evacuated and flushed with nitrogen three times, and three times evacuated and flushed with hydrogen. The resulting reaction mixture was then stirred for 1.5 h under an atmosphere of hydrogen at ambient pressure and temperature, prior to evacuation and ventilation with nitrogen. The reaction flask was opened to air, and the catalyst filtered off by suction over a pad of Celite. After removal of the solvent in a rotary evaporator under reduced pressure, the resulting crude product (8.07 g) was purified by flash chromatography (100 g of silica gel, pentane/ether, 1:1, Rf=0.28) to afford 4.28 g (55%) of (3Z,9Z)-2,7-dimethyltrideca-3,9-diene-2,5-diol as a colorless oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08278230B2uspto-grants-2012_10