Réaction #46168

ord-aa319d98b94f435396b145547cac0460

Solvants

Conditions de réaction

Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    ExtractionThe organic layer extracted with ethyl acetate
  2. 2
    Lavagewas washed with distilled water
  3. 3
    Séchagedried over anhydrous magnesium sulfate
  4. 4
    Concentrationconcentrated
  5. 5
    Autrethe resulting residue was purified by column chromatography (ethyl acetate:hexane=1:2)

Mode opératoire

1-Oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carbonitrile (200 mg, 0.547 mmol) was dissolved in ethanol. Hydroxy amine.hydrochloric acid (114 mg, 1.64 mmol) and pyridine (173 mg, 2.18 mmol) were added thereto and the mixture was stirred for 4 hours at 70° C. The organic layer extracted with ethyl acetate was washed with distilled water, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane=1:2) to obtain trails 1-hydroxy imino-3-phenyl-6-(3-phenylpropyloxy)-1H-indene-2-carbonitrile (95 mg, yield 45%) as a red solid,

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07741323B2uspto-grants-2010_06