Reacción #570650

ord-ea6bf6b283f04a6b8ca4c0ca02845c2f

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction mixture was heated
  2. 2
    Temperaturaat reflux overnight
  3. 3
    Extracciónextracted with ER (2×150 ml)
  4. 4
    Secadodried (Na2SO4) extracts
  5. 5
    Otrowere evaporated
  6. 6
    OtroThe residual oil was purified by flash chromatography over silica gel (Merck 9285, 5.0 cm wide column)
  7. 7
    Lavadoeluting with ER-CX (1:5→1:3)
  8. 8
    workup.DISTILLATIONThe resultant oil was further purified by distillation

Procedimiento

A Grignard reagent was prepared from 4-bromo-1-fluorobenzene (8.0 g), magnesium turnings (1.10 g), and iodine (one small crystal) in THF (40 ml). Oxetane (2.3 g) in THF (10 ml) was added at RT and the reaction mixture was heated at reflux overnight. The cooled solution was poured into aqueous saturated NH4Cl (100 ml), extracted with ER (2×150 ml) and the combined, dried (Na2SO4) extracts were evaporated. The residual oil was purified by flash chromatography over silica gel (Merck 9285, 5.0 cm wide column), eluting with ER-CX (1:5→1:3). The resultant oil was further purified by distillation to give the title compound (3.15 g) as a colourless oil, b.p. 150°/0.8 torr.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05225445uspto-grants-1993_07