Reacción #84753
ord-48efd38fab134ed9b2140e90274b5ab8
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroThe reaction was slowly quenched with methanol (50 mL)
- 2Otrothe solvents were removed under reduced pressure
- 3workup.ADDITIONThe residue was diluted with 200 mL of ethyl acetate
- 4Lavadowashed with water (200 mL) and brine (200 mL)
- 5Secadodried over sodium sulfate
- 6Filtraciónfiltered
- 7Concentraciónconcentrated
Procedimiento
To a solution of 6-amino-3-bromo-2-fluorobenzoic acid (9.0 g, 38.46 mmol) in THF (150 mL) was added BH3-THF (1 M, 193 mL) at 0° C., and the mixture was stirred at room temperature overnight. The reaction was slowly quenched with methanol (50 mL), and the solvents were removed under reduced pressure. The residue was diluted with 200 mL of ethyl acetate, washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered and concentrated to afford the title product (8.3 g, 98%), which was directly used in the next step without further purification. MS (ES+) C7H7BrFNO requires: 219, found: 220, 222 [M+H]+.