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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856683Generated: October 25, 2026

4-Nitropyridine N-oxide → 4-Ethoxypyridine n-oxide

https://huagongshe.com/reaction/856683

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitropyridine N-oxideHCID 14300—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product4-Ethoxypyridine n-oxideHCID 25247999%

Reaction Conditions

Temperature50 °C

Reaction Steps

4-nitropyridine-N-oxide (12 g) was dissolved in ethanol, sodium ethoxide (8.8 g) was added to the mixture, and the mixture was stirred for 40 hours at 50° C. After allowing the mixture to be cooled to room temperature, the precipitates were filtered, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give 4-ethoxypyridine-N-oxide (11.8 g). To 4-ethoxypyridine-N-oxide (11.8 g) was added dimethyl sulfate (8.56 ml), and the mixture was stirred for 1 hour at 110° C. After diluting with methanol (180 ml), the mixture was heated to reflux for 1 hour, an aqueous solution (18 ml) of ammonium peroxodisulfate (20.6 g) was added dropwise to the solution under heat reflux, and the mixture was heated to reflux for 1 hour. After allowing the mixture to be cooled to room temperature, the solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, to give (4-ethoxy-2-pyridinyl)methanol (2.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262185B2
Source datasetuspto-grants-2007_08
ORD IDord-ea5cc24d7f8e45ab98589abaa1ff7bc6
Source noteuspto-grants-2007_08