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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063308Generated: October 26, 2026

1-Benzyl-3,3-dimethylpiperidin-4-one → 3,3-Dimethylpiperidin-4-one

https://huagongshe.com/reaction/1063308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-3,3-dimethylpiperidin-4-oneHCID 9794413—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3,3-Dimethylpiperidin-4-oneHCID 2227883798.6%

Reaction Steps

1-Benzyl-3,3-dimethyl-4-piperidone 275 g (1.26 mol) prepared as per procedure described in U.S. Pat. No. 5,846,980, was dissolved in 1.0 L. methanol. The solution was transferred to a Parr reactor after adding 10% palladium on carbon (25 g). The reaction mixture was stirred under 300 psi hydrogen pressure at 60° C. until chromatography showed complete conversion. The reaction mixture was filtered and the residue washed with methanol (200 ml). The filtrate was concentrated to dryness to afford 3,3-dimethyl-4-piperidone (158 g) which was used as such for the preparation of either 4-benzyloxycarbonylamino-3,3-dimethylpiperidine or 4-t-butyloxycarbonylamino-3,3-dimethylpiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964966B2
Source datasetuspto-grants-2005_11
ORD IDord-91151967452b4d19a9912983af276fc2
Source noteuspto-grants-2005_11