반응 #49683

ord-94cc554d11ba4598bc45790c9073d60b

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was heated
  2. 2
    온도under reflux for 4 hours
  3. 3
    workup.ADDITIONthe mixture was poured onto ice (200 g)
  4. 4
    기타The layers were separated
  5. 5
    세척the organic layer was washed with 10% aqueous sodium carbonate (50 ml) and brine (50 ml)
  6. 6
    건조dried (MgSO4)
  7. 7
    농축concentrated in vacuo
  8. 8
    기타to give a colourless oil which
  9. 9
    기타The solid was chromatographed on silica eluting with ethyl acetate
  10. 10
    workup.ADDITIONcontaining hexane (20%)
  11. 11
    workup.ADDITIONThe fractions containing the less polar (higher Rf) product
  12. 12
    농축concentrated in vacuo

실험 절차

A solution of phosphorus tribromide (5 g) in carbon tetrachloride (10 ml) was added, dropwise, to a solution of 4-cyanophenethyl alcohol (8.06 g) in carbon tetrachloride (60 ml). The mixture was heated under reflux for 4 hours. On cooling to room temperature, the mixture was poured onto ice (200 g). The layers were separated and the organic layer was washed with 10% aqueous sodium carbonate (50 ml) and brine (50 ml), dried (MgSO4) and concentrated in vacuo to give a colourless oil which solidified on standing. The solid was chromatographed on silica eluting with ethyl acetate containing hexane (20%). The fractions containing the less polar (higher Rf) product were combined and concentrated in vacuo to give 4-cyanophenethyl bromide as a yellow oil which solidified on standing, yield 8.9 g. The fractions containing the more polar (lower Rf) product were combined and concentrated in vacuo to give the title compound as a colourless solid, yield 0.47 g, m.p. 152°-153° .

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05422358uspto-grants-1995_06