참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Isobutylene | HCID 8255 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Pyrazinecarbonitrile | HCID 73172 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | N-tert-butylpyrazine-2-carboxamide | HCID 4462842 | 6.6% |
반응 단계
575 g (5.75 mmol) of sulfuric acid was added dropwise to 900 ml of acetic acid over 35 minutes at 20° C. (cooling), followed by 200.1 g (1.9 mol) of cyanopyrazine over 20 minutes. 142.4 g (2.54 mol) of isobutene was then introduced over 3.5 hours, the temperature being kept below 25° C. by appropriate cooling. The mixture was subsequently stirred for a further 2 hours at room temperature and then poured into 1.8 l of ice-water. The mixture was brought to pH 3.5 by the slow addition of 1527 g of 30 percent sodium hydroxide solution and then extracted continuously for 4 hours with 2.5 l of hot methylcyclohexane in a liquid-liquid extractor. The extract was cooled to 4° C., with stirring, and the product which had crystallized out was filtered off and dried under vacuum. The yield of the title compound was 246 g, content (titration): 99.6 percent. Concentration of the mother liquor gave a further 22.5 g of the title compound with a content of 99.0 percent. The total yield of the title compound was 268.5 g (78 percent).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05945534 |
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| 출처 데이터셋 | uspto-grants-1999_08 |
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| ORD ID | ord-1ca05b56705d4c00a30c9ff1bfe4645a |
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| 출처 메모 | uspto-grants-1999_08 |
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