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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 856684Erstellt: 24. Oktober 2026

Dimethyl Sulfate → (4-Ethoxy-2-pyridinyl)methanol

https://huagongshe.com/de/reaction/856684

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktAmmonium PersulfateHCID 62648—
Edukt4-Ethoxypyridine n-oxideHCID 252479—
LösungsmittelMethanolHCID 887—
Produkt(4-Ethoxy-2-pyridinyl)methanolHCID 22938361—

Reaktionsbedingungen

Temperatur110 °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-ce64791831cc42288e852e1d04a1609c
Quellennotizuspto-grants-2007_08