Реакция #5807

ord-a9e5e1fe7109474dbd63453d82efc8ef

Уравнение реакции

O
water
CCOCC
diethyl ether
CC(C)(C)OC(=O)CC(=O)C[C@@H](CC#N)O[Si](C)(C)C(C)(C)C
(R)-1,1-dimethylethyl 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-oxohexanoate
CCCC[N+](CCCC)(CCCC)CCCC.[F-]
tetrabutylammonium fluoride
CC(C)(C)OC(=O)CC(=O)C[C@H](O)CC#N
(R)-1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate

Растворители

Условия реакции

Температура
25°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONis added
  2. 2
    Другоеthe layers separated
  3. 3
    СушкаThe organic layer is dried (magnesium sulfate)
  4. 4
    Фильтрацияfiltered through a plug of silica gel with the aid of anhydrous diethyl ether
  5. 5
    ДругоеThe solvent is removed under a vacuum

Методика

A solution of crude (R)-1,1-dimethylethyl 6-cyano-5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3-oxohexanoate, 43 g (0.126 mol) in 350 mL of tetrahydrofuran is treated with 213 mL of tetrabutylammonium fluoride solution (1.0M in hexane). The resulting mixture is stirred for five hours, at 25° C. The mixture is treated with 500 mL of water, 300 mL of diethyl ether is added, and the layers separated. The organic layer is dried (magnesium sulfate) and then filtered through a plug of silica gel with the aid of anhydrous diethyl ether. The solvent is removed under a vacuum to obtain 21 g of crude (R)-1,1-dimethylethyl 6-cyano-5-hydroxy-3-oxohexanoate with acceptable NMR, MS and IR spectra.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05245047uspto-grants-1993_09