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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 31567Erstellt: 24. Oktober 2026

Sodium hydride → 4-((5,5-Dimethyl-1,3-dioxan-2-yl)methoxy)-2,3-dimethylpyridine 1-oxide

https://huagongshe.com/de/reaction/31567

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt4-Chloro-2,3-dimethyl-1-oxidopyridin-1-iumHCID 9877446—
Edukt(5,5-Dimethyl-1,3-dioxan-2-yl)methanolHCID 59792511—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt4-((5,5-Dimethyl-1,3-dioxan-2-yl)methoxy)-2,3-dimethylpyridine 1-oxideHCID 5979255484,6%

Reaktionsschritte

The (5,5-dimethyl-1,3-dioxan-2-yl)methanol (2 g, 13.7 mmol) obtained in the step (1b) was mixed with sodium hydride in oil (822 mg, 20.6 mmol as the content was regarded as 60%) and dimethylsulfoxide (20 ml). The mixture was stirred at room temperature for 30 minutes. To the reaction mixture, 4-chloro-2,3-dimethylpyridine1-oxide (2.16 g, 13.7 mmol) was added and stirred at 50° C. overnight, and further allowed to stand still for one day at room temperature. After dimethylsulfoxide was distilled off, methanol and NH silica gel were added to the residue and then methanol was distilled off. The mixture of the reaction mixture and NH silica gel was purified by silica gel column chromatography (NH silica gel: 200 g, elution solvent: ethyl acetate/heptane=1/1 to 4/1→methanol/ethyl acetate=1/9) to obtain the title compound (3.1 g, yield: 84.6%) as a light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07425634B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-bceb0caeb4ea4f0ab7796a8402b3def5
Quellennotizuspto-grants-2008_09