반응 #168342

ord-50bc3f91e9504640a225aa39a785b91e

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타quenched with saturated NH4Cl solution
  2. 2
    기타The layers were separated
  3. 3
    추출the aqueous layer was extracted with EtOAc (2×10 mL)
  4. 4
    세척The combined organic layers were washed with brine
  5. 5
    건조dried over anhydrous Na2SO4
  6. 6
    여과filtered
  7. 7
    농축concentrated in vacuo
  8. 8
    기타Purification of the residue on a silica gel column (0 to 50% EtOAc/hexanes)

실험 절차

A solution of N-benzyl-2-chloro-N-((2R,3R)-2-hydroxypentan-3-yl)acetamide (210 mg, 0.7 mmol) in THF (5 mL) was added to a suspension of NaH (89 mg, 3.7 mmol) in THF (5 mL) at 0° C. The reaction mixture was stirred at 0° C. for 1 hour and then quenched with saturated NH4Cl solution. The layers were separated and the aqueous layer was extracted with EtOAc (2×10 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification of the residue on a silica gel column (0 to 50% EtOAc/hexanes) afforded (5R,6R)-4-benzyl-5-ethyl-6-methylmorpholin-3-one. MS APCl calc'd for C14H19NO2 [M+H]+ 234. found 234.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08846657B2uspto-grants-2014_09