関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | tert-Butanol | HCID 6386 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Pyrazinecarbonitrile | HCID 73172 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-tert-butylpyrazine-2-carboxamide | HCID 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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05734055 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-a23e58160f8d42ea84086afccb55201f |
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| 出典メモ | uspto-grants-1998_03 |
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