Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268172Generated: November 1, 2026

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

https://huagongshe.com/reaction/1268172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-nitrophenoxy)piperidine-1-carboxylateHCID 2794776—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylateHCID 2218115799.1%

Reaction Steps

To a solution of 4-(1-t-butoxycarbonylpiperidin-4-yloxy)nitrobenzene (11.9 g) in methanol (100 ml) was added palladium on carbon (1.9 g) and the mixture was stirred under a hydrogen atmosphere at room temperature for 4 hours. The reaction mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on a silica gel column using hexane/ethyl acetate=1/1 as an eluant to give the desired compound (10.7 g, yield 99%) as a pale red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555556B1
Source datasetuspto-grants-2003_04
ORD IDord-1935404a64aa4770a4d3ab9e658d742c
Source noteuspto-grants-2003_04