반응 #81618

ord-359ed0d63f8f41058fcdd48e27b873a8

용매

반응 조건

온도
68°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 1.5 hours
  2. 2
    기타evaporate the solvent in vacuo to a residue (700 mL)
  3. 3
    workup.STIRRINGAdd chloroform (1L) and stir until solids
  4. 4
    workup.DISSOLUTIONare dissolved
  5. 5
    기타Separate the organic phase
  6. 6
    추출extract the aqueous phase with chloroform (3×300 mL)
  7. 7
    건조Combine the organic phases, dry (MgSO4)
  8. 8
    기타evaporate the solvent in vacuo
  9. 9
    기타recrystallize (toluene)

실험 절차

Dissolve 4-[4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-1-oxobutyl]-2,2-dimethylphenethyl acetate (69.0 g, 0.131 mol) in methanol (2.5L) and add 10% aqueous sodium hydroxide (769 mL, 1.92 mol). Stir at reflux for 1.5 hours, cool to 68° C. and evaporate the solvent in vacuo to a residue (700 mL). Add chloroform (1L) and stir until solids are dissolved. Separate the organic phase and extract the aqueous phase with chloroform (3×300 mL). Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo and recrystallize (toluene) to give the title compound as a cream-colored powder; mp 135°-137° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05618940uspto-grants-1997_04