반응 #2839

ord-3e2d6cb3d26542d4af0ef67db3bb40ab

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe resulting mixture stirred
  2. 2
    온도at reflux for 6 hours
  3. 3
    온도After cooling
  4. 4
    기타the n-butanal was removed by evaporation
  5. 5
    workup.ADDITIONthe residue was treated with water (50 ml)
  6. 6
    추출extracted with dichloromethane (2×20 ml)
  7. 7
    세척washed with water (20 ml)
  8. 8
    건조dried (MgSO4)
  9. 9
    기타evaporated

실험 절차

Sodium hydride (60% w/v dispersion in mineral oil; 1.8 g) was added in portions over 20 minutes to n-butanol (100 ml) with stirring. The mixture was then stirred until no further hydrogen evolution was noted. 2,5-Dibromopyridine (7.1 g) was added and the resulting mixture stirred at reflux for 6 hours. After cooling, the n-butanal was removed by evaporation and the residue was treated with water (50 ml) and extracted with dichloromethane (2×20 ml). The organic extracts were combined, washed with water (20 ml), dried (MgSO4) and evaporated to give 5-bromo-2-n-butoxypyridine (6.3) as a pale yellow oil, NMR (DHSOd6): 0.9-0.96(3H, t), 1.32-1.5(2H, m), 1.62-1.76(2H, m), 4.2-4.28(2H, t), 6.79-6.82(1H, d), 7.85-7.9(1H, d of d) and 8.26(1H, d).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05731323uspto-grants-1998_03