Reacción #48045

ord-8cb30b2a5fa74259aa6b20b955ff6ebf

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat 0° C
  2. 2
    Extracciónthe resulting mixture was extracted with DCM
  3. 3
    LavadoThe combined organic extracts were washed with brine
  4. 4
    Secadodried (MgSO4)
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated in vacuo
  7. 7
    Otroto give a residue which
  8. 8
    Otrowas purified by flash column chromatography (100% pentane)

Procedimiento

To a solution of 5.66 g of 1-(4-bromophenyl)-cyclobutanol (24.92 mmol, described in example S2-A) in 70 ml DCM were added 4.23 g of (diethylamino)sulfur trifluoride (95%, 24.92 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 35 min, then sat. NaHCO3— solution was added and the resulting mixture was extracted with DCM. The combined organic extracts were washed with brine, dried (MgSO4), filtered, and concentrated in vacuo to give a residue which was purified by flash column chromatography (100% pentane) to give 1-bromo-4-(1-fluoro-cyclobutyl)-benzene (3.66 g, 64%) as a colorless liquid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07745477B2uspto-grants-2010_06