HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-4-piperidone → N-[(4-Methylphenyl)methyl]-1-(phenylmethyl)-4-piperidinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | 4-Methylbenzylamine | HCID 66035 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[(4-Methylphenyl)methyl]-1-(phenylmethyl)-4-piperidinamine | HCID 12146686 | — |
Reaction Steps
To a solution of 1-benzyl-4-piperidone (1.74 g, 9.2 mmol) and 4-methylbenzylamine (0.97 g, 8 mmol) in methanol (30 ml) was added sodium borohydride (525 mg) in small portions over 30 min. The reaction mixture was stirred at room temperature. After 16 h, the mixture was concentrated. Water (30 ml) was added, and the mixture was extracted with dichloromethane (2×20 ml). The combined organic layers were dried (Na2SO4), filtered, and concentrated to give 4-((4-methylphenyl)methyl)amino-1-phenylmethylpiperidine. The crude product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296694B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-1688deb06e164e35a1ef9284ceb5a98d |
| Source note | uspto-grants-2016_03 |