反応 #2146736

ord-f0c7fd6f53dd429eacba6619bfac7fb3

反応方程式

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
収率 55.1%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08278230B2uspto-grants-2012_10