Bromine → 2-Bromo-1-(4,5-dihydro-5-(2,6-difluorophenyl)-3-isoxazolyl)ethanone

Temperature

33 °C

To a 500-mL flask equipped with a mechanical stirrer, thermometer, addition funnel and scrubber were added 1-(4,5-dihydro-5-(2,6-difluorophenyl)-3-isoxazolyl)ethanone (i.e. the product of Step B) (60.0 g, 0.27 mmol) and dichloromethane (130 mL). The reaction mixture was heated at 33° C., and a solution of bromine (39.2 mL, 0.24 mol) in dichloromethane (100 mL) was added dropwise via the addition funnel. After about 5 mL of the bromine solution had been added, the addition was stopped and the reaction mixture was stirred at 33° C. for about 10 minutes, during which time the color of the reaction mixture changed from red to yellow. The reaction mixture was cooled to 5° C., and the remaining bromine solution was added dropwise over 90 minutes. After the addition was complete, the reaction mixture was washed with sodium bisulfite solution (3.5 g in 100 mL of water). The organic layer was concentrated under reduced pressure, hexanes were added, and the resulting solid precipitate was collected by filtration and washed with hexanes to provide the title compound as a brown solid (73 g), which was used without further purification

1. customTo a 500-mL flask equipped with a mechanical stirrer
2. additionthermometer, addition funnel
3. additionthe addition
4. temperatureThe reaction mixture was cooled to 5° C.
5. additionAfter the addition
6. washthe reaction mixture was washed with sodium bisulfite solution (3.5 g in 100 mL of water)
7. concentrationThe organic layer was concentrated under reduced pressure, hexanes
8. additionwere added
9. filtrationthe resulting solid precipitate was collected by filtration
10. washwashed with hexanes

ORD record

ord-cb8c89432fe34403909aee895745a9f8

Source dataset

uspto-grants-2013_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08349870B2