Реакция #159753

ord-989649abcefc4b8a9102d99a8a2c308c

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеwas brought to room temperature
  2. 2
    ДругоеThe reaction was quenched
  3. 3
    workup.ADDITIONby pouring it
  4. 4
    Другоеover crushed ice
  5. 5
    ЭкстракцияThe resulting mixture was extracted with dichloromethane
  6. 6
    ПромывкаThe organic layer was washed with aq. NaHCO3 (100 mL) and water (100 mL)
  7. 7
    Другоеthe solvent was evaporated
  8. 8
    Другоеto yield the crude product which
  9. 9
    Другоеwas 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).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08828951B2uspto-grants-2014_09