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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3648Generated: October 26, 2026

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

https://huagongshe.com/reaction/3648

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 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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05734055
Source datasetuspto-grants-1998_03
ORD IDord-b0a5f477af2d4178b1eacf13ac36441b
Source noteuspto-grants-1998_03