Реакция #1540
ord-2b0378d7412b4bedb3ed0ed2242b2a38
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Температура
120°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ТемператураThe mixture was cooled
- 2Промывкаwashed with two 100 mL portions of ether
- 3Фильтрацияthe precipitate was collected by filtration
- 4Другоеdried under vacuum at 50° C.
Методика
A mixture of 3.14 g (20.0 mmol) of benzamidine hydrochloride hydrate, 1.65 g (20.1 mmol) of powdered anhydrous sodium acetate, 4.17 g (22.2 mmol) of ethyl 3,3-diethoxyacrylate and 10 mL of DMSO was heated at 120° C. for 8 h. The mixture was cooled, diluted with 50 mL of 5% aqueous NaOH and washed with two 100 mL portions of ether. The aqueous layer was acidified with concentrated hydrochloric acid and the precipitate was collected by filtration and dried under vacuum at 50° C. to furnish 2.28 g (57%) of crude 6-ethoxy-2-phenyl-4(3H)-pyrimidinone as a yellow solid 1 H-NMR (d6-DMSO) δ 1.35(3H,t), 4.33(2H,q), 5.60(1H,s), 7.50(3H,m), 8.2(2H,m).