Reaction #1121803

ord-f7144b20ba7d4e028ba4c92d9d38229c

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe catalyst was removed by filtration
  2. 2
    Washwashed with methanol
  3. 3
    ConcentrationThe filtrate was concentrated

Procedure

Benzyl 3-(tert-butoxycarbonylamino)-3-methylpiperidine-1-carboxylate (1.4 g, 4.0 mmol) and 10% Pd/C (0.21 g, 0.2 mmol) in MeOH (20 mL) were stirred under H2 atmosphere (1 atm) for 1 hour. The catalyst was removed by filtration and washed with methanol. The filtrate was concentrated to give tert-butyl 3-methylpiperidin-3-ylcarbamate (0.62 g, 72% yield) as a solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08545897B2uspto-grants-2013_10