Реакция #68747
ord-6f7641894d3b4895a473f13086f5e497
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Экстракцияthe crude product is extracted with ethyl acetate (3×15 ml)
- 2Промывкаwashed with brine (10 ml)
- 3Сушкаdried over anhydrous magnesium sulfate
- 4Фильтрацияfiltered
- 5Другоеthe filtrate is evaporated to dryness under reduced pressure
Методика
A solution of 2-(4′-chloro-4-ethylbiphen-3-yl)-3-methoxycyclopent-2-enone (200 mg, 0.61 mmol) in acetone (4 ml) and 2M aqueous hydrochloric acid (4 ml) is heated at 120° C. for 20 minutes under microwave irradiation. The reaction mixture is diluted with water (20 ml) and 2M aqueous hydrochloric acid (10 ml), and the crude product is extracted with ethyl acetate (3×15 ml). The organic extracts are combined, washed with brine (10 ml), dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated to dryness under reduced pressure to give 2-(4′-chloro-4-ethylbiphen-3-yl)-1,3-cyclopentanedione.