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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 582245Erstellt: 24. Oktober 2026

Sulfuric Acid → N-tert-butylpyrazine-2-carboxamide

https://huagongshe.com/de/reaction/582245

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
Edukttert-ButanolHCID 6386—
EduktSodium HydroxideHCID 14798—
EduktPyrazinecarbonitrileHCID 73172—
LösungsmittelWaterHCID 962—
ProduktN-tert-butylpyrazine-2-carboxamideHCID 4462842—

Reaktionsschritte

To 1030 g of an 80% aqueous solution of sulfuric acid (8.40 moles of sulfuric acid), 220.5 g (2.10 moles) of 2-cyanopyrazine was added dropwise keeping the internal temperature at 40° C. or less with stirring. In succession, 187 g (2.52 moles) of tert-butyl alcohol was added dropwise to the mixture, keeping the internal temperature at 9° to 15° C., over 3 hours. Further, the temperature was kept at the same temperature for 2.5 hours. After the reaction, the reaction liquid was added to 3500 g of water with stirring. Thus obtained mixture was neutralized with an aqueous solution of sodium hydroxide. Precipitated crystalline solid was separated by filtration, washed with water and then dried to obtain 338.7 g (1.89 moles) of N-tert-butyl-2-pyrazine-carboxamide. It had a melting point of 88° to 90° C. Further, from the water layer, from which the intended product had been separated by filtration, 7.17 g (0.04 mole) of the intended product was further obtained by extraction thereof with toluene. Therefore, the yield of N-tert-butyl-2-pyrazinecarboxamide obtained here was 91.9%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05922873
Quelldatensatzuspto-grants-1999_07
ORD IDord-9fdadf8460a44268ad330e47232344a9
Quellennotizuspto-grants-1999_07