반응 #54347

ord-0587bcd743a44314873c72b7692035b6

용매

반응 조건

온도
25°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a -5° C.
  2. 2
    기타The reaction mixture is quenched by slow addition to 200 ml
  3. 3
    추출The quenched mixture is extracted with 250 ml
  4. 4
    세척of ether, the extract washed once with 200 ml
  5. 5
    건조20% potassium carbonate, dried over magnesium sulfate
  6. 6
    기타evaporated
  7. 7
    기타The residue is purified via column chromatography on 300 g
  8. 8
    세척silica gel eluted with 50% ether-cyclohexane

실험 절차

To a -5° C. solution of 3.0 g. (4.85 mmols.) of 1-benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]-4-(3-phenylpropyl)-4-piperidinol in 5 ml. of pyridine is slowly added 2.89 g. (24.3 mmols.) of thionyl chloride. The reaction mixture is then allowed to slowly warm to 25° C. and is stirred 12 hours longers. The reaction mixture is quenched by slow addition to 200 ml. of cold 20% potassium carbonate. The quenched mixture is extracted with 250 ml. of ether, the extract washed once with 200 ml. 20% potassium carbonate, dried over magnesium sulfate and evaporated. The residue is purified via column chromatography on 300 g. silica gel eluted with 50% ether-cyclohexane to yield the title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04147872uspto-grants-1979_04