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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387966Generated: November 1, 2026

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

https://huagongshe.com/reaction/1387966

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 numberUS06268354B1
Source datasetuspto-grants-2001_07
ORD IDord-3f33c6a9a0ba453585c011c82c1eb442
Source noteuspto-grants-2001_07