참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphoric Acid | HCID 1004 | — |
| 반응물 | Maleic Anhydride | HCID 7923 | — |
| 반응물 | Dodecylamine | HCID 13583 | — |
| 반응물 | 2-Methoxy-1,4-benzoquinone | HCID 76146 | — |
| 촉매 | Zinc Acetate | HCID 11192 | — |
| 용매 | Tetralin | HCID 8404 | — |
| 생성물 | 1H-Pyrrole-2,5-dione, 1-dodecyl- | HCID 87191 | — |
반응 단계
The same reactor as used in Example 7 was adopted. In this reactor, a solution of 120 g of maleic anhydride in 360 g of tetrahydronaphthalene was placed. Then, a solution of 220 g of dodecylamine and 1760 g of tetrahydronaphthalene was added thereto at 40° C. over a period of 120 minutes. After the addition was completed, the resultant mixture and 65.4 g of ortho-phosphoric acid (purity 89% by weight), 1.344 g of methoxybenzoquinone, and 0.1 g of zinc acetate added thereto were heated at 210° C. for one hour to effect reaction. Thereafter, the resultant reaction mixture was cooled to 30° C. and separated into a water layer and a tetrahydronaphthalene layer. The tetrahydronaphthalene layer was distilled to expel tetrahydronaphthalene. Consequently, there was obtained 285 g of slightly impure N-dodecyl maleimide. It was found to have purity of 92.3% by weight, indicating the yield thereof to be 83.5 mol % based on dodecylamine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04780546 |
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| 출처 데이터셋 | uspto-grants-1988_10 |
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| ORD ID | ord-a656e95f3f9749a89d4dce64cc03a074 |
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| 출처 메모 | uspto-grants-1988_10 |
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