Реакция #6649
ord-6b77fd970be54f8dbe3fb67395b6565b
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1ДругоеThe organic layer was separated
- 2Экстракцияthe aqueous layer was extracted with 2×50 ml of hexanes
- 3Промывкаwashed successively with 30 ml of water and 2×30 ml of saturated NaCl solution
- 4Сушкаdried (MgSO4)
- 5ДругоеThe solvent was removed in vacuo
- 6Другоеthe residue purified by recrystallization from an ethyl acetate and hexanes mixture
Методика
To a solution of 9.48 g (80 mmol) of 3,3-dimethylacryloyl chloride in 200 ml of dry THF was added with vigorous shaking a solution of 13.76 g (80 mmol) of 4-bromoaniline in 300 ml of dry THF. The mixture was stood at room temperature for 2 h and then treated with 80 g of ice followed by 200 ml of hexane. The organic layer was separated and the aqueous layer was extracted with 2×50 ml of hexanes. The organic layers were combined and washed successively with 30 ml of water and 2×30 ml of saturated NaCl solution and then dried (MgSO4). The solvent was removed in vacuo and the residue purified by recrystallization from an ethyl acetate and hexanes mixture to give the title compound as colorless crystals. PMR (CDCl3): δ 1.91 (3H, s), 2.23 (3H, s), 5.73 (1H, broad s), 7.38-7.55 (5H, m).