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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066992Generated: October 30, 2026

1-Benzyl-4-methyl-4-phenylpiperidine → 4-Methyl-4-phenylpiperidine

https://huagongshe.com/reaction/1066992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-methyl-4-phenylpiperidineHCID 10801662—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-Methyl-4-phenylpiperidineHCID 3019511110.8%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245773B1
Source datasetuspto-grants-2001_06
ORD IDord-db282d10447f4da3b06e3e2f5f8e46d4
Source noteuspto-grants-2001_06