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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1077839Erstellt: 23. Oktober 2026

m-Chloroperbenzoic acid → 2-(4-methylphenyl)-6-methylpyridine-N-oxide

https://huagongshe.com/de/reaction/1077839

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt2-Methyl-6-(4-methylphenyl)pyridineHCID 603081—
LösungsmittelChloroformHCID 6212—
Produkt2-(4-methylphenyl)-6-methylpyridine-N-oxideHCID 1943033057,2%

Reaktionsschritte

A solution of 2-(4-methylphenyl)-6-methylpyridine (4.5 g) in 100 ml of chloroform was cooled to 0° C., and m-chloroperbenzoic acid (7.7 g) in 50 ml of chloroform was added over a period of 15 minutes. The mixture was stirred at room temperature for 3 hours, then at 50° C. for 2 hours, followed by stirring overnight at room temperature. Solvent was evaporated to a small volume under reduced pressure, and the residue passed through an alumina column, eluting with 2% methanol in methylene chloride to remove benzoic acid. The eluate was flash-chromatographed on silica gel, eluting with 5% methanol in methylene chloride, to yield 2.8 g of 2-(4-methylphenyl)-6-methylpyridine-N-oxide, m.p. 95° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05545645
Quelldatensatzuspto-grants-1996_08
ORD IDord-6666939eed814061b84f82f13e26e1cd
Quellennotizuspto-grants-1996_08