Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121632Generated: October 25, 2026

1-(1-Benzyloxycarbonyl-4-piperidinylmethyl)-4-(t-butoxycarbonylamino)piperidine → 4-(t-Butoxycarbonylamino)-1-(4-piperidinylmethyl)piperidine

https://huagongshe.com/reaction/2121632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Benzyloxycarbonyl-4-piperidinylmethyl)-4-(t-butoxycarbonylamino)piperidineHCID 12986153—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-(t-Butoxycarbonylamino)-1-(4-piperidinylmethyl)piperidineHCID 12986154101.6%

Reaction Steps

To a solution of 1-(1-benzyloxycarbonyl-4-piperidinylmethyl)-4-(t-butoxycarbonylamino)piperidine (10.0 g) in ethanol (100 ml) and water (10 ml) is added a 10% palladium-on-carbon (1.2 g), and the mixture is reduced at a room temperature under at a moderate pressure (3.0 kg/cm2). After the consumption and disappearance of the starting compound is confirmed (about 2 hours thereafter), the catalyst is removed by filtration. The filtrate is evaporated under reduced pressure to give crude 4-(t-butoxycarbonylamino)-1-(4-piperidinyl-methyl)piperidine (about 7 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696468B2
Source datasetuspto-grants-2004_02
ORD IDord-78363785c6bf493b8469762628835900
Source noteuspto-grants-2004_02