Reacción #10306

ord-c1acfb3adf39446d8b5e3103b040d2f4

Condiciones de reacción

Temperatura
80°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe cooled reaction mixture
  2. 2
    workup.ADDITIONadded
  3. 3
    Otroto obtain
  4. 4
    Otroan easier separation of the 2 layers
  5. 5
    LavadoThe organic layer was washed with brine
  6. 6
    Secadodried (MgSO4)
  7. 7
    Concentraciónconcentrated
  8. 8
    OtroThe residue was purified on a plug of silica eluting with 3% EtOAc/isohexane

Procedimiento

To a solution of 2-bromo-5-fluorotoluene (5 g, 26.5 mmol) in DMF (65 ml) and water (15 ml) was added butyl vinyl ether (6.6 g, 65.9 mmol), palladium acetate (0.18 g, 0.8 mmol), 1,3-bis(diphenylphosphino)propane (0.72 g, 1.75 mmol) and potassium carbonate (4.4 g, 31.8 mmol). The reaction was heated at 80° C. for 48 h under nitrogen. The cooled reaction mixture was diluted with EtOAc (˜250 ml) and concentrated HCl added and shaken. Further EtOAc and water were added to obtain an easier separation of the 2 layers. The organic layer was washed with brine, dried (MgSO4), and concentrated. The residue was purified on a plug of silica eluting with 3% EtOAc/isohexane to give the title compound as an oil (1.95 g, 49%). 1H NMR (400 MHz, d6-DMSO) δ 2.45 (3H, s), 2.54 (3H, s), 7.13–7.17 (2H, m), 7.89–7.93 (1H, m).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07094777B2uspto-grants-2006_08