반응 #1537894

ord-3982c9c2c12d4a81b6160ac1f3292f86

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과After filtration of the catalyst
  2. 2
    기타through cellite and evaporation of the solvent
  3. 3
    workup.ADDITIONTherefore 0.6 g of Pearlman's catalyst was added in 40 ml ethanol (95%) once more
  4. 4
    workup.ADDITIONthe mixture was treated under H2 -atmosphere at 0.28 MPa over night
  5. 5
    여과Filtration
  6. 6
    기타through cellite and evaporation of the solvent
  7. 7
    기타gave the product in a quantitative yield (2.18 g)

실험 절차

3.1 g (0.01 mol) (3RS)-1-benzyl-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine was hydrogenated at 0.28 MPa over 0.6 g of Pearlman's catalyst (Pd(OH)2) in 40 ml ethanol (95%) over night. After filtration of the catalyst through cellite and evaporation of the solvent 1H-NMR showed that the reaction was not completed. Therefore 0.6 g of Pearlman's catalyst was added in 40 ml ethanol (95%) once more and the mixture was treated under H2 -atmosphere at 0.28 MPa over night. Filtration through cellite and evaporation of the solvent gave the product in a quantitative yield (2.18 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05602253uspto-grants-1997_02