Quinoline → (9Z)-7-methyltrideca-9-ene-2,5-diol

HRID 1799156Notes

Reaction equation

HRID 1799156 reaction equation
N1C2C(=CC=CC=2)C=CC=1.[CH3:11][CH:12]([CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH3:26])[CH2:13][CH:14]([OH:20])[C:15]#[C:16][CH:17]([OH:19])[CH3:18]>C(O)C.[Pd]>[CH3:11][CH:12]([CH2:21]/[CH:22]=[CH:23]\[CH2:24][CH2:25][CH3:26])[CH2:13][CH:14]([OH:20])[CH2:15][CH2:16][CH:17]([OH:19])[CH3:18]

Participants

5

Procedure

At room temp., 550 mg (0.516 mmol) of 10% palladium on barium sulphate and 200 mg (1.55 mmol) of quinoline were added to a stirred solution of 7.60 g (33.9 mmol) of this (9Z)-7-methyltridec-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 2 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 (6.87 g) was purified by flash chromatography (100 g of silica gel, pentane/ether, 1:1, Rf=0.10) to afford 6.15 g (80%) of (9Z)-7-methyltrideca-9-ene-2,5-diol as a colorless oil.

Workup

  1. customThe flask was evacuated
  2. customflushed with nitrogen three times, and three times
  3. customevacuated
  4. customflushed with hydrogen
  5. customThe resulting reaction mixture
  6. filtrationthe catalyst filtered off by suction over a pad of Celite
  7. customAfter removal of the solvent
  8. customin a rotary evaporator under reduced pressure
  9. customthe resulting crude product (6.87 g) was purified by flash chromatography (100 g of silica gel, pentane/ether, 1:1, Rf=0.10)

Sources & evidence

ORD record
ord-ef49a31a5ad947d283a7320d31957c52
Source dataset
uspto-grants-2013_01
Patent number
US08344023B2

Reaction notes

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