HRID21684

反应详情

EQUATION

反应方程式

HRID 21684 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Methyl 8-(N-Cbz-amino)-3-oxo-octanoate (3,51.5 g, 0.16 moles) was dissolved in anhydrous tetrahydrofuran (350 mL) in a reaction flask equipped with a magnetic stirbar, reflux condenser, pressure equalizing addition funnel and nitrogen gas inlet. While stirring the mixture under nitrogen sodium borohydride (15.1 g, 0.4 moles) was cautiously added. The mixture was then heated to reflux and methanol was added dropwise over 90 minutes. Stirring was continued at reflux temperature for 60 minutes after the addition was complete. After allowing the solution to cool to ambient temperature, distilled water (78 mL) was added and 3N HCl was added to pH 3. The mixture was evaporated in vacuo to remove the organic solvents, and solid potassium carbonate was added to adjust the pH back to 12. The mixture was then extracted with ethyl acetate (5×100 mL). The extract was washed with saturated sodium chloride (2×50 mL), dried over sodium sulfate, filtered and evaporated in vacuo. The residue was dissolved in methanol (200 mL) and evaporated again. This was repeated a total of five times. The residue was crystallized from ether (700 mL) giving 8-(N-Cbz-amino)-1,3-octanediol (4,23 g). A second crop was collected on addition of cyclohexane (300 mL) to the mother liquor (6.8 g). Mass Spectrum: (M+H)+ (M+H)+ @m/z 296, (M+H4)+ @m/z 313.

WORKUP

后处理

  1. customequipped with a magnetic stirbar
  2. temperaturereflux condenser
  3. additionaddition funnel and nitrogen gas inlet
  4. additionwas cautiously added
  5. temperatureThe mixture was then heated
  6. temperatureto reflux
  7. stirringStirring
  8. temperatureat reflux temperature for 60 minutes
  9. additionafter the addition
  10. distillationdistilled water (78 mL)
  11. additionwas added
  12. addition3N HCl was added to pH 3
  13. customThe mixture was evaporated in vacuo
  14. customto remove the organic solvents, and solid potassium carbonate
  15. additionwas added
  16. extractionThe mixture was then extracted with ethyl acetate (5×100 mL)
  17. washThe extract was washed with saturated sodium chloride (2×50 mL)
  18. dry with materialdried over sodium sulfate
  19. filtrationfiltered
  20. customevaporated in vacuo
  21. dissolutionThe residue was dissolved in methanol (200 mL)
  22. customevaporated again
  23. customThe residue was crystallized from ether (700 mL)