참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfate | HCID 6497 | — |
| 반응물 | 1-Aminoanthraquinone | HCID 6710 | — |
| 반응물 | Nitrobenzene | HCID 7416 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 촉매 | Acetic Acid | HCID 176 | — |
| 촉매 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Solvent Red 111 | HCID 6706 | 99.5% |
반응 단계
A mixture of 1-aminoanthraquinone (purity 99.6%, 22.4 g), nitrobenzene (224 g), 96% potassium hydroxide (11.7 g), tetra-n-butyl ammonium bromide (1.7 g) and dimethylsulfuric acid (25 g) was stirred, while being maintained at 30° C. for 24 hours. Then, after water (150 g) was added, the solution was stirred for one hour while being maintained at 50° C. The aqueous phase had pH of 10 or higher. After acetic acid (0.5 g) was added for neutralization until pH of the aqueous phase was 7, nitrobenzene was recovered. The solution was cooled down to 50° C., and filtered. The solid material was washed and dried, to obtain 1-methylaminoanthraquinone (23.7 g, purity: 99.5%, yield 99.5%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05017713 |
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| 출처 데이터셋 | uspto-grants-1991_05 |
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| ORD ID | ord-d9e53a716ba04b998f9de63b4b3c8d8b |
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| 출처 메모 | uspto-grants-1991_05 |
|---|