Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 3648Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/3648

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 of which internal temperature was kept at 9° to 15° C. over 3 hours. Further, the temperature was kept at the same temperature for 2.5 hours. After that, the reaction liquid was poured into 3500 g of water with stirring. Thus obtained mixture was neutralized with an aqueous solution of sodium hydroxide. The precipitated crystalline solid was separated by filtration, washed with water and dried to obtain 338.7 g (1.89 moles) of N-tert-butyl-2-pyrazinecarboxamide. It had a melting point of 88° to 90° C. Further, from the filtrate 7.17 g (0.04 mole) of N-tert-butyl-2-pyrazine-carboxamide was further obtained by extraction thereof with toluene. The yield thereof was 91.9%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05734055
Quelldatensatzuspto-grants-1998_03
ORD IDord-b0a5f477af2d4178b1eacf13ac36441b
Quellennotizuspto-grants-1998_03