1-Benzyl-4-methyl-4-phenylpiperidine → 4-Methyl-4-phenylpiperidine
Reaction equation
C([N:8]1[CH2:13][CH2:12][C:11]([CH3:20])([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:10][CH2:9]1)C1C=CC=CC=1.[H][H]>CO.[Pd]>[CH3:20][C:11]1([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH2:10][CH2:9][NH:8][CH2:13][CH2:12]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a cooled suspension of 10% Pd-C (0.5 g) in 10 mL methanol was added a solution of 1-benzyl-4-methyl-4-phenylpiperidine (4.5 g, 17.0 mmol) in 40 mL of methanol and the resulting suspension was hydrogenated in a Parr bomb under 250 psi of hydrogen for two days. The suspension was filtered through a pad of celite and the solvent was removed from the filtrate to obtain 4-methyl-4-phenylpiperidine as a yellow solid (3.3 g, 99% yield).
Workup
- filtrationThe suspension was filtered through a pad of celite
- customthe solvent was removed from the filtrate
Sources & evidence
- ORD record
- ord-db282d10447f4da3b06e3e2f5f8e46d4
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06245773B1
Reaction notes
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