반응 #49683
ord-94cc554d11ba4598bc45790c9073d60b
반응 조건
후처리
- 1온도The mixture was heated
- 2온도under reflux for 4 hours
- 3workup.ADDITIONthe mixture was poured onto ice (200 g)
- 4기타The layers were separated
- 5세척the organic layer was washed with 10% aqueous sodium carbonate (50 ml) and brine (50 ml)
- 6건조dried (MgSO4)
- 7농축concentrated in vacuo
- 8기타to give a colourless oil which
- 9기타The solid was chromatographed on silica eluting with ethyl acetate
- 10workup.ADDITIONcontaining hexane (20%)
- 11workup.ADDITIONThe fractions containing the less polar (higher Rf) product
- 12농축concentrated 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° .