Reacción #45297

ord-b8617ab280b7493fb302a5cd3f3e2cdc

Ecuación de reacción

O
water
O
water
CC(C)(C)N
t-Butylamine
CC(Br)C(=O)c1cccc(Cl)c1
m-chloro-α-bromopropiophenone
CC(C)(C)N
t-butylamine
CC(NC(C)(C)C)C(=O)c1cccc(Cl)c1.Cl
bupropion hydrochloride

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction mixture was refluxed for 2.5 hours
  2. 2
    Otrowas evaproated at the temperature of 120° C
  3. 3
    Extracciónextracted with 1500 ml of chloroform and 250 ml of water
  4. 4
    SecadoThe organic phase was dried with anhydrous sodium sulfate (30 g)
  5. 5
    Concentraciónconcentrated to dryness under reduced pressure
  6. 6
    workup.ADDITIONA solution of HCl in ethanol was added to the concentrated solution at room temperature

Procedimiento

t-Butylamine was added to a solution of m-chloro-α-bromopropiophenone obtained above in acetone and water and the reaction mixture was refluxed for 2.5 hours. Acetone, water and excessive t-butylamine was evaproated at the temperature of 120° C. The concentrated solution was cooled down to room temperature and then extracted with 1500 ml of chloroform and 250 ml of water. The organic phase was dried with anhydrous sodium sulfate (30 g) and concentrated to dryness under reduced pressure. A solution of HCl in ethanol was added to the concentrated solution at room temperature and a crude product of bupropion hydrochloride was obtained after filtration. The crude product of bupropion hydrochloride was added to 2000 ml ethanol and heated to 70° C., decolorized by activated carbon (2 g) for 30 minutes and filtered. The filtrate was cooled and filtered to obtain wet product of bupropion hydrochloride. The wet product was dried in vacuum (−0.04˜−0.09 MPa, 70° C.) for 4 hours to obtain pure product. Total yield was 72% based on m-chloropropiophenone; and the HPLC's purify was ≧99.9%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07737302B2uspto-grants-2010_06