Reacción #2146736

ord-f0c7fd6f53dd429eacba6619bfac7fb3

Ecuación de reacción

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
Rendimiento 55.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08278230B2uspto-grants-2012_10