반응 #81618
ord-359ed0d63f8f41058fcdd48e27b873a8
반응 방정식
반응물
시약
없음
용매
반응 조건
온도
68°CELSIUS
상세 조건
See reaction.notes.procedure_details.
후처리
- 1온도at reflux for 1.5 hours
- 2기타evaporate the solvent in vacuo to a residue (700 mL)
- 3workup.STIRRINGAdd chloroform (1L) and stir until solids
- 4workup.DISSOLUTIONare dissolved
- 5기타Separate the organic phase
- 6추출extract the aqueous phase with chloroform (3×300 mL)
- 7건조Combine the organic phases, dry (MgSO4)
- 8기타evaporate the solvent in vacuo
- 9기타recrystallize (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.