Реакция #68004

ord-4a786edb6cba4750b7f60d17b93ce9d9

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvent was removed under reduced pressure
  2. 2
    Экстракцияextracted with ethyl acetate
  3. 3
    ПромывкаThe organic layer was washed sequentially with water
  4. 4
    Сушкаan aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate
  5. 5
    Другоеthe solvent was removed under reduced pressure

Методика

Into 3 mL of a 90% aqueous trifluoroacetic acid solution, 156 mg of 1-(1,3-dioxolan-2-ylmethyl)-4-chloroquinolin-2(1H)-one was dissolved, and the mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure, and the reaction mixture was alkalified with an aqueous saturated sodium hydrogen carbonate solution, and then extracted with ethyl acetate. The organic layer was washed sequentially with water and an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 192 mg of a pale yellow oily substance, (4-chloro-2-oxoquinolin-1(2H)-yl)acetaldehyde.

Источник

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