Реакция #472717
ord-dfd2f72356074fdd9d8fe6e947f8561e
Уравнение реакции
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураunder cooling with ice
- 2ДругоеThe organic layer was separated
- 3Промывкаwashed with an aqueous sodium chloride solution
- 4Сушкаdried over anhydrous magnesium sulfate
- 5workup.DISTILLATIONthe solvent was distilled off under reduced pressure
Методика
To 184 mL of 80% trifluoroacetic acid, 4.60 g of 1-(1,3-dioxolan-2-ylmethyl)-7-methoxy-1,5-naphthyridin-2(1H)-one was dissolved, and the resultant solution was stirred at room temperature for 11 hours and at 60° C. for 3.5 hours. The reaction mixture was charged with chloroform and alkalified with a 10% aqueous sodium hydroxide solution under cooling with ice. The organic layer was separated, and washed with an aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain (7-methoxy-2-oxo-1,5-naphthyridin-1(2H)-yl)acetaldehyde as a yellow solid.