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HRID 3648作成日:2026年10月25日

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

https://huagongshe.com/reaction/3648

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物tert-ButanolHCID 6386—
反応物Sodium HydroxideHCID 14798—
反応物PyrazinecarbonitrileHCID 73172—
溶媒WaterHCID 962—
生成物N-tert-butylpyrazine-2-carboxamideHCID 4462842—

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05734055
出典データセットuspto-grants-1998_03
ORD IDord-b0a5f477af2d4178b1eacf13ac36441b
出典メモuspto-grants-1998_03