참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | 2,4-Diaminotoluene | HCID 7261 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Maleic Anhydride | HCID 7923 | — |
| 반응물 | Magnesium chloride hexahydrate | HCID 24644 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 1H-Pyrrole-2,5-dione, 1,1'-(4-methyl-1,3-phenylene)bis- | HCID 80893 | 85% |
반응 단계
A flask was equipped as in Example 1. To a solution of maleic anhydride (1.7 parts) in 3.9 parts acetone was added a solution of 1 part 4-methyl-m-phenylenediamine, 0.28 part triethylamine and 2.5 parts acetone. The heterogeneous reaction mixture was stirred at 40° C. for 30 minutes. Magnesium chloride hexahydrate (0.071 part) and 2.16 part acetic anhydride were added all at once. The reaction temperature was raised to 50° C. and maintained for 2.5 hours. Thirty minutes after the addition the mixture became homogeneous and remained so. The solution was cooled, and 16 parts water was added; the precipitated product was filtered by vacuum filtration, washed with water, and dried in a vacuum oven at 60° C. for 24 hours. N,N'-(4-Methyl-m-phenylene)dimaleimide, m.p. 168°-172° C., was obtained in 85% yield.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04154737 |
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| 출처 데이터셋 | uspto-grants-1979_05 |
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| ORD ID | ord-42c1bcf76c544651a422c1274a989376 |
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| 출처 메모 | uspto-grants-1979_05 |
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