Reacción #7919

ord-92a03a8e4c1e41349e525d8248b38466

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe mixture was filtered
  2. 2
    Otrothe filtrate evaporated under vacuum
  3. 3
    OtroThe residue was partitioned between EtOAc (200 mL) and water (200 mL)
  4. 4
    workup.ADDITIONcontaining 2N HCl (5 mL)
  5. 5
    LavadoThe organic phase was washed with brine (100 mL)
  6. 6
    Secadodried over MgSO4
  7. 7
    Filtraciónfiltered
  8. 8
    Otroevaporated under vacuum

Procedimiento

Potassium hydroxide (0.44 g, 85% weight pure, 6.67 mmol) and 10% palladium on activated carbon (0.42 g) were added to a mixture of 5-methoxy-1-indanone (5.0 g, 30.8 mmol) and butyraldehyde (3.3 mL, 37 mmol) in ethanol (30 mL). The resulting mixture was stirred under an atmosphere of hydrogen at room temperature for 2 hours. The mixture was filtered and the filtrate evaporated under vacuum. The residue was partitioned between EtOAc (200 mL) and water (200 mL) containing 2N HCl (5 mL). The organic phase was washed with brine (100 mL), dried over MgSO4, filtered, and evaporated under vacuum to afford crude 2-butyl-5-methoxy-1-indanone (7.0 g) as an oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087599B2uspto-grants-2006_08