Reacción #5327

ord-b2e4e352ee244261996ff42a33ea5c0d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGwas stirred for 5 hours at 100° C
  2. 2
    OtroThe reaction mixture was partitioned between ethyl acetate and water
  3. 3
    ExtracciónThe aqueous layer was extracted with ethyl acetate
  4. 4
    Lavadowashed with water
  5. 5
    Otrodried
  6. 6
    Otrothe solvent was evaporated in vacuo
  7. 7
    OtroThe residue was purified by column chromatography on silica gel

Procedimiento

To a solution of hydroxylamine hydrochloride (17.9 g) in dimethyl sulfoxide (120 ml) was added a methanol solution of sodium methoxide prepared from metallic sodium (5.92 g) and anhydrous methanol (50 ml). The mixture was stirred for 10 minutes at room temperature, to which was added 2'-cyano-4-methylbiphenyl (10 g) The reaction mixture was stirred for 5 hours at 100° C. The reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate. Organic layers were combined, washed with water and dried, then the solvent was evaporated in vacuo. The residue was purified by column chromatography on silica gel to afford the title compound as a white amorphous product (11.2 g, 96%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05243054uspto-grants-1993_09