Реакция #159753
ord-989649abcefc4b8a9102d99a8a2c308c
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Другоеwas brought to room temperature
- 2ДругоеThe reaction was quenched
- 3workup.ADDITIONby pouring it
- 4Другоеover crushed ice
- 5ЭкстракцияThe resulting mixture was extracted with dichloromethane
- 6ПромывкаThe organic layer was washed with aq. NaHCO3 (100 mL) and water (100 mL)
- 7Другоеthe solvent was evaporated
- 8Другоеto yield the crude product which
- 9Другоеwas recrystallized from hot ethylacetate
Методика
To an ice cooled solution of 5-bromo-2-chlorobenzoyl chloride in dichloromethane (35 mL) was added 1-(2,3-dihydro-benzo[1,4]oxazin-4-yl)-2,2,2-trifluoro-ethanone (6.5 g, 28.1 mmol) in dichloromethane (45 mL) followed by AlCl3 (5.61 g, 42.2 mmol) portion wise. After 2 h, the reaction mixture was brought to room temperature and stirred overnight. The reaction was quenched by pouring it over crushed ice. The resulting mixture was extracted with dichloromethane. The organic layer was washed with aq. NaHCO3 (100 mL) and water (100 mL), and the solvent was evaporated to yield the crude product which was recrystallized from hot ethylacetate to furnish 1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone (10.0 g).