Tert-Butyl isocyanide → 4-Methoxyoxane-4-carbonitrile

HRID 2389290ノート

反応式

HRID 2389290 の反応式
CO[C:3]1([O:9][CH3:10])[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.[C:11]([N+:15]#[C-])(C)(C)C.C(=O)([O-])O.[Na+]>ClCCl.[Ti](Cl)(Cl)(Cl)Cl>[CH3:10][O:9][C:3]1([C:11]#[N:15])[CH2:4][CH2:5][O:6][CH2:7][CH2:8]1

参加物

6

反応条件

温度
-78 °C

実験手順

Under an argon atmosphere, 4,4-dimethoxytetrahydropyran (4.39 g, 30.0 mmol) was dissolved in dichloromethane (60 mL), and tert-butyl isocyanide (3.73 mL, 33.0 mmol) and titanium tetrachloride (3.95 mL, 36.8 mmol) were added thereto at −78° C., and then, the mixture was stirred overnight at room temperature. To the mixture, an aqueous sodium hydrogen carbonate solution was added, and the mixture was filtered through Celite, and then, the filtrate was extracted with chloroform. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20) to give 4-methoxytetrahydropyran-4-carbonitrile (3.30 g, 23.4 mmol, yield: 78%).

後処理

  1. filtrationthe mixture was filtered through Celite
  2. extractionthe filtrate was extracted with chloroform
  3. washThe organic layer was washed with saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20)

出典と根拠

ORDレコード
ord-48983d2434924313ac37912bcec33dbf
出典データセット
uspto-grants-2012_09
特許番号
US08273738B2

反応ノート

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