Reaktion #159753

Reaktionsgleichung

AlCl3

5-bromo-2-chlorobenzoyl chloride

1-(2,3-dihydro-benzo[1,4]oxazin-4-yl)-2,2,2-trifluoro-ethanone

→

1-[6-(5-bromo-2-chloro-benzoyl)-2,3-dihydro-benzo[1,4]oxazin-4-yl]-2,2,2-trifluoro-ethanone

Lösungsmittel

dichloromethane

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigewas brought to room temperature
2. 2
   SonstigeThe reaction was quenched
3. 3
   workup.ADDITIONby pouring it
4. 4
   Sonstigeover crushed ice
5. 5
   ExtraktionThe resulting mixture was extracted with dichloromethane
6. 6
   WaschenThe organic layer was washed with aq. NaHCO3 (100 mL) and water (100 mL)
7. 7
   Sonstigethe solvent was evaporated
8. 8
   Sonstigeto yield the crude product which
9. 9
   Sonstigewas recrystallized from hot ethylacetate

Vorschrift

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).

Quelle