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HRID 582245作成日:2026年10月26日

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

https://huagongshe.com/reaction/582245

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, 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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05922873
出典データセットuspto-grants-1999_07
ORD IDord-9fdadf8460a44268ad330e47232344a9
出典メモuspto-grants-1999_07