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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3648생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물tert-ButanolHCID 6386—
반응물Sodium HydroxideHCID 14798—
반응물PyrazinecarbonitrileHCID 73172—
용매WaterHCID 962—
생성물N-tert-butylpyrazine-2-carboxamideHCID 4462842—

반응 단계

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%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05734055
출처 데이터셋uspto-grants-1998_03
ORD IDord-b0a5f477af2d4178b1eacf13ac36441b
출처 메모uspto-grants-1998_03