반응 #630390

ord-2059ff4320184caa89158e76fd251f53

반응 방정식

O=C(O)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
6-Hydroxy-2(S)-phthalimidohexanoic acid
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
O=C(OCc1ccccc1)[C@H](CCCCO)N1C(=O)c2ccccc2C1=O
benzyl 6-hydroxy-2(S)-phthalimidohexanoate
수율 198.6%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Most of the methanol was removed in vacuo
  2. 2
    기타the resulting aqueous residue was freeze-dried
  3. 3
    workup.DISSOLUTIONThe lyophilized material was dissolved in DMF (70 ml)
  4. 4
    workup.ADDITIONtreated with 3.08 g of benzyl bromide
  5. 5
    workup.STIRRINGAfter stirring under nitrogen for 6 hours
  6. 6
    workup.ADDITIONthe reaction mixture was diluted with 450 ml of water
  7. 7
    추출repeatedly extracted with ethyl acetate
  8. 8
    세척Organic layers were then back-washed with water
  9. 9
    건조dried (Na2SO4)
  10. 10
    농축concentrated

실험 절차

6-Hydroxy-2(S)-phthalimidohexanoic acid (5.0 g) was dissolved in a mixture of 90 ml of methanol and 9 ml of water. To this solution, an aqueous 0.5M cesium carbonate solution (18 ml) was added and the mixture stirred for a few minutes. Most of the methanol was removed in vacuo and the resulting aqueous residue was freeze-dried. The lyophilized material was dissolved in DMF (70 ml) and treated with 3.08 g of benzyl bromide. After stirring under nitrogen for 6 hours, the reaction mixture was diluted with 450 ml of water and repeatedly extracted with ethyl acetate. Organic layers were then back-washed with water, dried (Na2SO4), and concentrated to give 6.58 g of benzyl 6-hydroxy-2(S)-phthalimidohexanoate. Recrystallization from ether gave a white solid, m.p. 106.5°-108°; [α]D25° =-27.6° (MeOH, c=1.77).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04661479uspto-grants-1987_04