反応 #5807

ord-a9e5e1fe7109474dbd63453d82efc8ef

反応方程式

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

反応条件

温度
25°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONis added
  2. 2
    その他the layers separated
  3. 3
    乾燥The organic layer is dried (magnesium sulfate)
  4. 4
    ろ過filtered through a plug of silica gel with the aid of anhydrous diethyl ether
  5. 5
    その他The solvent is removed under a vacuum

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05245047uspto-grants-1993_09