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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584267Generated: October 25, 2026

tert-Butyl 3-azidopiperidine-1-carboxylate → 1-BOC-3-Aminopiperidine

https://huagongshe.com/reaction/1584267

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-azidopiperidine-1-carboxylateHCID 547722—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product1-BOC-3-AminopiperidineHCID 545809—

Reaction Steps

A solution of 3-azido-N-t-butoxycarbonylpiperidine (850 mg) in ethyl acetate (50 ml) was hydrogenated in the presence of 10% Pd/C (550 mg) at atmospheric pressure for 2.5 h. The reaction mixture was then filtered through Celite and the filtrate concentrated in vacuo to give the title compound. 1H NMR (CDCl3) d 1.46 (s, 9 H), 1.66-2.05 (m, 4 H), 2.57 (br s, 1 H), 2.78 (m, 4 H), 3.80 (br d, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932606
Source datasetuspto-grants-1999_08
ORD IDord-6545213480014f10b07d078d49433929
Source noteuspto-grants-1999_08