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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482565Generated: October 25, 2026

Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate → 4-(N-Boc-amino)piperidine

https://huagongshe.com/reaction/482565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylateHCID 21981786—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(N-Boc-amino)piperidineHCID 723833100%

Reaction Steps

N-CBZ-4-(BOC-amino)-piperidine (3.0 g, 9.0 mmol) was dissolved in ethanol (100 mL) and transferred into a Parr shaker bottle. After adding 10% palladium on carbon (0.5 g), the mixture was shaken under an atmosphere of hydrogen at 50 psi for 0.75 h on a Parr apparatus. The catalyst was removed by filtration through a pad of Celite. The filter cake was washed with ethanol and the combined filtrate and washings were concentrated in vacuo to yield 1.8 g (100%) of crude 4-(BOC-amino)-piperidine as a pale yellow oil. This product was used immediately in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798337
Source datasetuspto-grants-1998_08
ORD IDord-e44a2a2a49a9468baf915e63b5283c87
Source noteuspto-grants-1998_08