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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268202Generated: November 1, 2026

4-(1-t-Butoxycarbonylpiperidin-4-yloxy)-3-isopropylnitrobenzene → 4-(1-t-Butoxycarbonylpiperidin-4-yloxy)-3-isopropylaniline

https://huagongshe.com/reaction/1268202

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-t-Butoxycarbonylpiperidin-4-yloxy)-3-isopropylnitrobenzeneHCID 18542642—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-(1-t-Butoxycarbonylpiperidin-4-yloxy)-3-isopropylanilineHCID 1854259274.4%

Reaction Steps

To a solution of 4-(1-t-butoxycarbonylpiperidin-4-yloxy)-3-isopropylnitrobenzene (4.1 g) in methanol (70 ml) was added palladium on carbon (0.4 g) and the mixture was stirred under a hydrogen atmosphere at room temperature for 3 hours. The reaction mixture was filtered and the filtrate concentrated in vacuo. The residue was purified by chromatography on a silica gel column using hexane/ethyl acetate=3/2 as an eluant to give the desired compound (2.8 g, yield 74%) as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555556B1
Source datasetuspto-grants-2003_04
ORD IDord-b87cb19541454d72b6b68276cc4dc481
Source noteuspto-grants-2003_04