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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611217Generated: November 1, 2026

Benzyl 3-(tert-butoxycarbonylamino)piperidine-1-carboxylate → 3-(Boc-amino)piperidine

https://huagongshe.com/reaction/1611217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 3-(tert-butoxycarbonylamino)piperidine-1-carboxylateHCID 22258937—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(Boc-amino)piperidineHCID 423304191%

Reaction Steps

A mixture of benzyl 3-[(tert-butoxycarbonyl)amino]-1-piperidinecarboxylate (2.25 g, 6.73 mmol) and 10% Pd/C (0.229 g) in EtOH (20 mL) was stirred at room temperature under a hydrogen atmosphere (1 atm) for 14 hrs. The catalyst was removed by filtration through Celite®, and the filtrate was concentrated under reduced pressure to give tert-butyl 3-piperidinylcarbamate as a solid (1.22 g, yield; 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984649B1
Source datasetuspto-grants-2006_01
ORD IDord-51eb60e552e34c49a224322ce3df2687
Source noteuspto-grants-2006_01