Tert-butyl 3-azidoazetidine-1-carboxylate → Tert-butyl 3-aminoazetidine-1-carboxylate
Reaction equation
[C:1]([O:5][C:6]([N:8]1[CH2:11][CH:10]([N:12]=[N+]=[N-])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>C(O)C.[Pd]>[C:1]([O:5][C:6]([N:8]1[CH2:11][CH:10]([NH2:12])[CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred solution of the azide (1.15 g, 5.80 mmol, Example 317) in ethanol (20 mL), 10% palladium on carbon (93 mg) was added and the mixture was hydrogenated for 1 hour at 48 psi. The mixture was filtered through a pad of celite and the solvent was removed to a colorless oil. 940 mg, 94%. The compound was directly used for the next step.
Workup
- filtrationThe mixture was filtered through a pad of celite
- customthe solvent was removed to a colorless oil
Sources & evidence
- ORD record
- ord-7fbc6ab19fd348728571777cb29fcede
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07615634B2
Reaction notes
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