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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 856683Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/856683

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Nitropyridine N-oxideHCID 14300—
EduktSodium ethoxideHCID 2723922—
LösungsmittelEthanolHCID 702—
Produkt4-Ethoxypyridine n-oxideHCID 25247999%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07262185B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-ea5cc24d7f8e45ab98589abaa1ff7bc6
Quellennotizuspto-grants-2007_08