Реакция #68003

ord-78eecf72391849b98a90421fdba3ea0d

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvent was removed under reduced pressure, and ethyl acetate
  2. 2
    workup.ADDITIONan aqueous saturated sodium hydrogen carbonate solution were added
  3. 3
    ДругоеThe organic layer was separated
  4. 4
    Экстракцияthe aqueous layer was extracted with ethyl acetate
  5. 5
    Промывкаthe resultant solution was washed with an aqueous saturated sodium chloride solution
  6. 6
    Сушкаdried over anhydrous magnesium sulfate
  7. 7
    Другоеthe solvent was removed under reduced pressure

Методика

To 0.42 g of 1-(1,3-dioxolan-2-ylmethyl)-6-isopropylquinolin-2(1H)-one, 4 mL of a 90% aqueous trifluoroacetic acid solution was added, and the mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure, and ethyl acetate and an aqueous saturated sodium hydrogen carbonate solution were added thereto. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 0.41 g of a pale yellow oily substance, (6-isopropyl-2-oxoquinolin-1(2H)-yl)acetaldehyde.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08524738B2uspto-grants-2013_09