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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277211Generated: October 31, 2026

2-((4-Nitrobenzyl)oxy)tetrahydro-2H-pyran → 4-(2-Tetrahydropyranyloxymethyl)aniline

https://huagongshe.com/reaction/1277211

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-((4-Nitrobenzyl)oxy)tetrahydro-2H-pyranHCID 10900655—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(2-Tetrahydropyranyloxymethyl)anilineHCID 1847219776%

Reaction Steps

To a solution of 4-(2-tetrahydropyranyloxymethyl)nitrobenzene (59.7 g, 0.256 mol) in ethanol (EtOH) (300 ml) was added under nitrogen atmosphere at room temperature 10% Pd/C (5.97 g), and catalytic hydrogenation was carried out. The mixture was stirred at room temperature for 24 hours. After the reaction completed, the catalyst was filtered off, and the organic layer was concentrated under reduced pressure. The residue was purified with silica gel column chromatography to give 4-(2-tetrahydropyranyloxymethyl)aniline (39.7 g, 76%) as syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166006
Source datasetuspto-grants-2000_12
ORD IDord-84ef5f0c89a643618b9d6c217104ba8f
Source noteuspto-grants-2000_12