Reaktion #79340

ord-53ddd933fc464c58bafcb5d535a76f82

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was equipped with a Dean Stark trap
  2. 2
    workup.ADDITIONcontaining 4.0 angstrom molecular sieves
  3. 3
    Temperaturrefluxed for 16 h
  4. 4
    SonstigeThe reaction was transferred to a separatory funnel
  5. 5
    workup.ADDITIONcontaining
  6. 6
    Extraktionextracted with EtOAc (3×100 mL)
  7. 7
    WaschenThe combined organics were washed with H2O, brine
  8. 8
    Trocknendried over Na2SO4
  9. 9
    Einengenconcentrated
  10. 10
    SonstigeThe resulting oil was purified by column chromatography

Vorschrift

Ethylene glycol (25.6 mL, 458 mmol) and p-toluenesulfonic acid (4.36 g, 22.9 g) were added to a solution of 1-(2-bromo-5-fluorophenyl)ethanone (10.5 g, 45.8 mmol) stirring in benzene (250 mL). The reaction mixture was equipped with a Dean Stark trap containing 4.0 angstrom molecular sieves and refluxed for 16 h. The reaction was transferred to a separatory funnel containing a 1:1 mixture of H2O and sat. NaHCO3 (aq) and extracted with EtOAc (3×100 mL). The combined organics were washed with H2O, brine, dried over Na2SO4 and concentrated. The resulting oil was purified by column chromatography to give 2-(2-bromo-5-fluorophenyl)-2-methyl-1,3-dioxolane (7.20 g) in 58% yield. 1H NMR (CDCl3, 300 MHz) δ2.60 (s, 3 H) 4.02-4.20 (m, 4H), 6.85-6.90 (m, 1H), 7.29-7.33 (m, 1H), 7.48-7.56 (m, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06713471B1uspto-grants-2004_03