Reacción #1605767

ord-79a5d3ab3ec74432bab0d13458ac7c2b

Ecuación de reacción

CC(=O)[O-].[Na+]
sodium acetate
COc1ccc2c(c1)CCC2=O
5-Methoxy-2,3-dihydromden-1-one
Cl.NO
hydroxylamine HCl
COc1ccc2c(c1)CCC2=NO
5-methoxy-2,3-dihydroinden-1-one oxime

Condiciones de reacción

Temperatura
70°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas brought up to 70° C.
  2. 2
    Otroto produce a precipitate
  3. 3
    workup.STIRRINGto stir for 2 h
  4. 4
    FiltraciónThe precipitate was collected by filtration

Procedimiento

5-Methoxy-2,3-dihydromden-1-one (Ig, 6.17 mmol) was added to a solution of hydroxylamine HCl (730 mg, 10.5 mmol) in 10 ml of water. The mixture was brought up to 70° C. and a solution of sodium acetate (1.4 g, 16.7 mmol) in 7 mL of H2O, 14 ml of MeOH, 3 ml of THF was added. After stirring for 1.5 h at 70° C., 10 ml of H2O was added to produce a precipitate and the suspension was allowed to stir for 2 h. The precipitate was collected by filtration to give 5-methoxy-2,3-dihydroinden-1-one oxime almost quantitatively and was used in the next step without further purification. The oxime (0.5 g, 2.82 mmol) was dissolved in MeOH and a catalytic amount of Raney nickel and 25 mL of ammonia solution in MeOH (7N) was added. The reaction was stirred at r.t. overnight under H2. The slurry was filtered over celite and concentrated in vacuo, diluted with EtOAc, washed with water and brine, dried over MgSO4, filtered, and concentrated in vacuo to give the crude title amine (yield, 45%). The crude amine was used without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09072313B2uspto-grants-2015_07