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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929693Generated: October 30, 2026

1-Benzyl-4-piperidone → N-[(4-Methylphenyl)methyl]-1-(phenylmethyl)-4-piperidinamine

https://huagongshe.com/reaction/929693

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
Reactant4-MethylbenzylamineHCID 66035—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductN-[(4-Methylphenyl)methyl]-1-(phenylmethyl)-4-piperidinamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296694B2
Source datasetuspto-grants-2016_03
ORD IDord-a9db2d0fd27b424382782cd174809f3c
Source noteuspto-grants-2016_03