Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 727917Erstellt: 26. Oktober 2026

Water → 4-(4-Methoxybutoxy)-2-methylpyridine 1-oxide

https://huagongshe.com/reaction/727917

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-Butanol, 4-methoxy-HCID 8107—
EduktSodium hydrideHCID 24758—
Edukt4-Chloro-2-methyl-1-oxo-1lambda~5~-pyridineHCID 12211801—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt4-(4-Methoxybutoxy)-2-methylpyridine 1-oxideHCID 1516621574,8%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

6.77 g (0.065 mol) of 4-methoxybutanol was dissolved in 60 ml of dimethyl sulfoxide to obtain a solution. 2.6 g (0.065 mol) of 60% sodium hydride was added to this solution at a room temperature in a nitrogen atmosphere. The obtained mixture was heated to 60° C., stirred for one hour and cooled to a room temperature. A solution of 4.66 g (0.032 mol) of 4-chloro-2-methylpyridine 1-oxide in 20 ml of dimethyl sulfoxide was dropwise added to the resulting mixture. The obtained mixture was stirred at 40° C. for one hour. After the completion of the reaction, 5 ml of water was added to the mixture and the obtained mixture was evaporated to dryness to remove the solvent. 150 ml of water was added to the residue. The obtained mixture was extracted with 200 ml of chloroform four times. The extract was dried over magnesium sulfate and filtered. The filtrate was distilled to remove the solvent. The residue was purified by silica gel column chromatography (ethyl acetate/methanol) to obtain 5.06 g of the title compound as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05045552
Quelldatensatzuspto-grants-1991_09
ORD IDord-0b98370f18c54259b33f9462456d4a0e
Quellennotizuspto-grants-1991_09