تفاعل #80263

معادلة التفاعل

Methyl 8-(N-Cbz-amino)-3-oxo-octanoate

methyl 8-(N-Cbz-amino)-3-oxo-octanoate

methanol

→

8-(N-Cbz-amino)-1,3-octanediol

المردود 48.7%

المذيبات

tetrahydrofuran

ظروف التفاعل

المعالجة

1. 1
   أخرىequipped with a magnetic stirbar
2. 2
   درجة الحرارةreflux condenser
3. 3
   workup.ADDITIONaddition funnel and nitrogen gas inlet
4. 4
   workup.ADDITIONwas cautiously added
5. 5
   درجة الحرارةThe mixture was then heated
6. 6
   درجة الحرارةto reflux
7. 7
   workup.STIRRINGStirring
8. 8
   درجة الحرارةat reflux temperature for 60 minutes
9. 9
   workup.ADDITIONafter the addition
10. 10
    workup.DISTILLATIONdistilled water (78 mL)
11. 11
    workup.ADDITIONwas added
12. 12
    workup.ADDITION3N HCl was added to pH 3
13. 13
    أخرىThe mixture was evaporated in vacuo
14. 14
    أخرىto remove the organic solvents, and solid potassium carbonate
15. 15
    workup.ADDITIONwas added
16. 16
    استخلاصThe mixture was then extracted with ethyl acetate (5×100 mL)
17. 17
    غسيلThe extract was washed with saturated sodium chloride (2×50 mL)
18. 18
    تجفيفdried over sodium sulfate
19. 19
    ترشيحfiltered
20. 20
    أخرىevaporated in vacuo
21. 21
    workup.DISSOLUTIONThe residue was dissolved in methanol (200 mL)
22. 22
    أخرىevaporated again
23. 23
    أخرىThe residue was crystallized from ether (700 mL)

الإجراء التجريبي

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+NH4)+ @m/z 313.

المصدر