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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357576Erstellt: 24. Oktober 2026

Dimethyl Sulfoxide → 4-(3-Methoxypropoxy)-2,3,5-trimethylpyridine 1-oxide

https://huagongshe.com/de/reaction/357576

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktSodium hydrideHCID 24758—
Edukt4-Chloro-2,3,5-trimethyl-1-oxidopyridin-1-iumHCID 2779141—
EduktPropylene glycol methyl etherHCID 3032390—
Produkt4-(3-Methoxypropoxy)-2,3,5-trimethylpyridine 1-oxideHCID 15166217—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

4.5 g (0.05 mol) of methoxypropanol was dissolved in 45 ml of dimethyl sulfoxide to obtain a solution. 2.0 g 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. and stirred for one hour. After the completion of the reaction, a solution of 4.3 g (0.025 mol) of 4-chloro-2,3,5-trimethylpyridine 1-oxide in 15 ml of dimethyl sulfoxide was dropwise added to the reaction mixture at a room temperature. The obtained mixture was stirred at 60° C. for 5 hours, cooled and distilled to dryness to remove the solvent. 200 ml of water was added to the obtained residue. The obtained mixture was extracted with 150 ml of chloroform five 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/n-hexane) to obtain 4.27 g of the title compound as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05840910
Quelldatensatzuspto-grants-1998_11
ORD IDord-1d58406a8b994aa7b63e9078ecd96c75
Quellennotizuspto-grants-1998_11