Reacción #964
ord-2326e4f1e4844936a51646b96ee23d0d
Ecuación de reacción
(3RS)-1-benzyl-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine
→
(3RS)-3-(N-tert-butyloxycarbonylaminoethyl) pyrrolidine
Reactivos
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1FiltraciónAfter filtration of the catalyst
- 2Otrothrough cellite and evaporation of the solvent
- 3workup.ADDITIONTherefore 0.6 g of Pearlman's catalyst was added in 40 ml ethanol (95%) once more
- 4workup.ADDITIONthe mixture was treated under H2 -atmosphere at 0.28 MPa over night
- 5FiltraciónFiltration
- 6Otrothrough cellite and evaporation of the solvent
- 7Otrogave the product in a quantitative yield (2.18 g)
Procedimiento
3.1 g (0.0t 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).