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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747774Generated: October 29, 2026

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

https://huagongshe.com/reaction/747774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(4-nitrophenoxy)piperidine-1-carboxylateHCID 2794776—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylateHCID 22181157—

Reaction Steps

2.74 g (8.5 mmol) of 1-t-butoxycarbonyl-4-(4-nitrophenoxy)piperidine was dissolved in 20 ml of ethanol. 20 mg of 10% palladium/carbon was added to the solution, and they were stirred at room temperature in 1 atm. hydrogen atmosphere for 3 hours. Palladium/carbon was removed by the suction filtration. The filtrate was once concentrated and then treated with dichloromethane as extractant in an ordinary manner to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396844B1
Source datasetuspto-grants-2008_07
ORD IDord-aca25c323e6c47a5a53c06ec71df4fe2
Source noteuspto-grants-2008_07