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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700296Generated: October 31, 2026

Tert-butyl 4-(4-nitrophenoxy)piperidine-1-carboxylate → tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1700296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-nitrophenoxy)piperidine-1-carboxylateHCID 2794776—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Producttert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylateHCID 2218115785.5%

Reaction Steps

A slurry of 4-(N-(t-butoxycarbonyl)piperidin-4-yl)oxy-1-nitrobenzene (15.1 g, 46.8 mmol) in absolute ethanol (500 mL) and methanol (200 mL) was purged with nitrogen, treated with 10% palladium on carbon (1.2 g, 50% water by wt.) and placed on a Parr Hydrogenator under 43 psi of hydrogen gas. The catalyst was removed by filtration. Solvent removal under reduced pressure gave a solid after drying. Purification by flash silica gel chromatography using a step gradient of 50 to 85% ethyl acetate in hexane gave 11.7 g of 4-(N-(t-butoxycarbonyl)piperidin-4-yl)oxybenzenamine, NMR (CDCl3, TMS) δ1.45 (s, 9), 1.7 (m, 2), 1.86 (m, 2), 3.25 (m, 2), 3.68 (m, 2), 4.25 (m, 1), 6.63 (m, 2), 6.76 (m, 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350761B1
Source datasetuspto-grants-2002_02
ORD IDord-9120f7165cca456ca394b3e9d85fe046
Source noteuspto-grants-2002_02