Реакция #65746

ord-c122d6c730f541f4a3dcfbcfd6f66660

Растворители

Условия реакции

Температура
150°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияthe mixture was extracted with ethyl acetate
  2. 2
    ПромывкаThe organic layer was washed with water
  3. 3
    Сушкаa saturated aqueous solution of sodium chloride, and dried over magnesium sulfate
  4. 4
    workup.DISTILLATIONThe solvent was distilled off
  5. 5
    Другоеthe residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane 1:2)
  6. 6
    Другоеto give an oily product

Методика

To 1.0 g of 3,4-diethoxycarbonyl-5-nitro-6-phenyl-2-pyridone was added 1.3 ml (3.37 eq.) of phenylphosphonic dichloride, and the mixture was heated at 150° C. for 2.5 hours. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane 1:2), to give an oily product. Yield: 950 mg (90.5%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05420275uspto-grants-1995_05