참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | N-Butylphthalimide | HCID 73812 | — |
| 생성물 | 2-Butyl-5-nitro-1H-isoindole-1,3(2H)-dione | HCID 93297 | — |
| 생성물 | 1H-Isoindole-1,3(2H)-dione, 2-butyl-4-nitro- | HCID 4547910 | — |
반응 단계
A 3-necked, 5-liter round-bottomed flask, equipped with a mechanical stirrer, was charged with 4,259 g (67.6 moles) of 99% nitric acid. To the flask was added 524.9 g (2.58 moles) N-butylphthalimide as a liquid at such a rate as to keep the reaction temperature under 40° C. The addition of the N-butylphthalimide was completed in about a half hour. The reaction was then heated for six hours to 50° C. in a temperature controlled water bath. The reaction product was then fed to a wiped film evaporator that was heated at 100° C. and under vacuum (30 mm). The bulk of the nitric acid was distilled off and the liquid product, i.e., 4-nitro-N-butylphthalimide and 3-nitro-N-butylphthalimide in a ratio of about 25:1, was isolated as a liquid which rapidly solidified to about 98% solids upon cooling in the collection vessel. Depending on the operation of the evaporator, the residual nitric acid in the product was less than 3% by weight, and was as low as 0.1% by weight
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06008374 |
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| 출처 데이터셋 | uspto-grants-1999_12 |
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| ORD ID | ord-3c82667ae3fc43feb3ee48a5615550fd |
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| 출처 메모 | uspto-grants-1999_12 |
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