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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582245Generated: October 26, 2026

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

https://huagongshe.com/reaction/582245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactanttert-ButanolHCID 6386—
ReactantSodium HydroxideHCID 14798—
ReactantPyrazinecarbonitrileHCID 73172—
SolventWaterHCID 962—
ProductN-tert-butylpyrazine-2-carboxamideHCID 4462842—

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922873
Source datasetuspto-grants-1999_07
ORD IDord-9fdadf8460a44268ad330e47232344a9
Source noteuspto-grants-1999_07