Reaktion #645104

ord-d91de79d30b54d8caa2f6f96865bd9a2

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvents were evaporated
  2. 2
    workup.ADDITIONgas-filled-balloon for 3 h
  3. 3
    FiltrationThe mixture was filtered
  4. 4
    Einengenthe filtrate was concentrated

Vorschrift

1-tert-Butyl 2-methyl (2S)-4-hydroxy-4-phenylpyrrolidine-1,2-dicarboxylate (0.32 g, 0.0010 mol) was treated with trifluoroacetic acid (1.00 mL, 0.0130 mol) and methylene chloride (1.00 mL, 0.0156 mol) at rt for 4 h. The solvents were evaporated and the residue was dissolved in methanol (5.0 mL, 0.12 mol). Palladium (50.0 mg, 0.000470 mol) was added under nitrogen and the resulting mixture was hydrogenized with a hydrogen-gas-filled-balloon for 3 h. The mixture was filtered and the filtrate was concentrated to give the desired product, which was directly used in the next step without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08058288B2uspto-grants-2011_11