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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353322Erstellt: 25. Oktober 2026

Potassium Carbonate → 2-Methylquinoxaline

https://huagongshe.com/reaction/353322

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
EduktSodium AcetateHCID 517045—
EduktSodium;hydrogen sulfite;oxaldehydeHCID 23706077—
EduktOrthotoluylendiaminHCID 55283794—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt2-MethylquinoxalineHCID 23686—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 122 g of ortho-toluenediamine (1.0 mole) dissolved in 500 cc of 2 M acetic acid, 250 cc of 4 M sodium acetate solution was added with stirring. The mixture was heated up to 60° C. and poured rapidly into a solution of 298.4 g (1.05 moles) of sodium glyoxal bisulfite in 1500 cc of water previously heated to 60° C. The resulting dark solution was stirred for one hour and it was then cooled down in an ice bath until the temperature had dropped below 10° C. The solution was then neutralized with 120 g of sodium hydroxide pellets. After the sodium hydroxide had dissolved, 500 g of potassium carbonate was added. During the addition of alkali, the solution turned red and a black oil separated out. Most of the oily amine was removed by extraction with pentane or hexane and the combined organic phase was dried over MgSO4, filtered and vacuum dried to give a brown oil that upon distillation gave methyl-quinoxaline (92 g) as a clear pale yellow to colorless liquid (80% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06750343B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-c926f4c1a1d245e7adeba4806c0597cf
Quellennotizuspto-grants-2004_06