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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896512Generated: October 29, 2026

tert-Butyl 3-(azidomethyl)piperidine-1-carboxylate → 1-Boc-3-(aminomethyl)piperidine

https://huagongshe.com/reaction/896512

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-(azidomethyl)piperidine-1-carboxylateHCID 22647380—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Boc-3-(aminomethyl)piperidineHCID 275648396%

Reaction Steps

A mixture of 3-azidomethylpiperidine-1-carboxylic acid tert-butyl ester (5.0 g, 20.8 mmol), ethanol (125 mL) and 10% palladium on charcoal (1.5 g) was shaken under a hydrogen atmosphere (60 psig) for 5 hours. The mixture was filtered. The filtrate was concentrated to provide a colorless oil (4.27 g, 96%) which was used without further purification. 1H NMR (300 MHz, CDCl3) δ3.91 (b, 1H), 3.82 (dt, J=13, 4 Hz, 1H), 2.90 (m, 1H), 2.8-2.5 (m, 3H), 1.85 (m, 1H), 1.75 (s, 2H), 1.66 (m, 1H), 1.6-1.4 (m, 2H), 1.47 (s, 9H), 1.20 (m, 1H). Mass spec (AP+) m/z 215.2 (M+H+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919356B2
Source datasetuspto-grants-2005_07
ORD IDord-9545baed5c254b2cafc3c4a7c2ca9033
Source noteuspto-grants-2005_07