Реакция #5767

ord-afd51883db244e12b7b5da102322d549

Уравнение реакции

O
water
CC1=CC=C(C(C)C)C(=O)CC(C)=CCCC(C)=CCC1
2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-cyclotetradecatetraen-1-one
CC(C)[CH2][Al+][CH2]C(C)C.[H-]
diisobutyl aluminium hydride
CCCCCC.CCOC(C)=O
hexane ethyl acetate
C/C1=C\C=C(\C(C)C)[C@@H](O)C/C(C)=C/CC/C(C)=C/CC1
sarcophytol A
Выход 90.3%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеOne hour
  2. 2
    Сушкаby drying over MgSO4, filtration, and concentration
  3. 3
    Другоеto give a residue, which

Методика

To the above ketone compound, 2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-cyclotetradecatetraen-1-one (137 mg, 0.48 mmol) in dry toluene (2.5 ml) was dropwise added with stirring on a cooling bath at -70° C. a solution of 1M diisobutyl aluminium hydride in toluene (0.6 ml). One hour later, disappearance of the starting material was confirmed. After addition of water (0.25 ml) and removal of the cooling bath, the reaction mixture was stirred, followed by drying over MgSO4, filtration, and concentration to give a residue, which was subjected to silica gel column chromatography (solvent:-hexane/ethyl acetate=12:1) to obtain the aimed sarcophytol A (125 mg, 88%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05245085uspto-grants-1993_09