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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20222Generated: October 26, 2026

Benzyl 4-(2-oxoazepan-1-yl)piperidin-1-carboxylate → 1-(Piperidin-4-yl)azepan-2-one

https://huagongshe.com/reaction/20222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-(2-oxoazepan-1-yl)piperidin-1-carboxylateHCID 68418576—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-(Piperidin-4-yl)azepan-2-oneHCID 68417512101%

Reaction Steps

To a solution of benzyl 4-(2-oxoazepan-1-yl)piperidin-1-carboxylate (0.25 g) obtained in Example 9a) in ethanol (10 mL) was added 10% palladium on carbon (containing 50% water; 0.03 g), and the mixture was stirred at room temperature for 15 hours under a hydrogen atmosphere. The reaction mixture was filtered, and the solvent was distilled off under reduced pressure to obtain the title compound (0.15 g, quantitative) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745623B2
Source datasetuspto-grants-2010_06
ORD IDord-6fd8d293355045979e6505dd8785f092
Source noteuspto-grants-2010_06