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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2220238Erstellt: 26. Oktober 2026

Carbon Dioxide → 2-Methyl-5-nitroquinoline

https://huagongshe.com/reaction/2220238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktNitrateHCID 943—
EduktNitric AcidHCID 944—
Edukt2-MethylquinolineHCID 7060—
EduktSodium HydroxideHCID 14798—
EduktPotassium NitrateHCID 24434—
EduktAzane;hydrateHCID 12896473—
LösungsmittelSulfuric AcidHCID 1118—
Produkt2-Methyl-5-nitroquinolineHCID 294867—

Reaktionsschritte

2-Methylquinoline (108.3 ml, 0.80 mol) is added in drops to 65% nitric acid (61 ml, 0.88 mol) at an internal temperature of 0-10° C. (dry ice cooling) within 45 minutes. After 1 hour, the precipitated nitrate is suctioned off and introduced in portions at an internal temperature of 0-6° C. in concentrated sulfuric acid (240 ml). After 30 minutes, potassium nitrate (6 g, 60 mmol) is added thereto, and it is stirred for 16 hours at room temperature. The batch is slowly poured onto ice/water, and a pH of 1.5 is set with 40% NaOH (˜500 ml). The precipitate is suctioned off, the filtrate is made alkaline with 25% ammonia water (pH 10) and filtered. The filter residue is dissolved in hot methanol (500 ml). During cooling, the 8-nitro-isomer crystallizes out. The mother liquor is concentrated by evaporation and purified by column chromatography on silica gel with hexane-ethyl acetate, whereby 53 g of the 2-methyl-5-nitroquinoline accumulates.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07417056B2
Quelldatensatzuspto-grants-2008_08
ORD IDord-2b3023a3a5554417b4edaac830ddc58f
Quellennotizuspto-grants-2008_08