関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 9,10-Anthracenedione, 1-amino-2-chloro-4-hydroxy- | HCID 75590 | — |
| 反応物 | N,N-di-n-octyl-m-aminophenol | HCID 15734569 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Anthraquinone | HCID 6780 | — |
反応手順
One part of 1-amino-2-chloro-4-hydroxyanthraquinone, 10 parts of 1,3-dimethyl-2-imidazolidinone, 1.0 part of potassium carbonate and 2.0 parts of N,N-di-n-octyl-m-aminophenol were mixed at room temperature, and then heated to 150° C. While this temperature was maintained, the reaction was conducted for 5 hours. The reaction mixture was cooled, then charged into 100 parts of water, extracted with toluene and thereafter purified through silica gel column chromatography to obtain an anthraquinone compound as coloring matter No. 1 (yield 90%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06800674B2 |
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| 出典データセット | uspto-grants-2004_10 |
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| ORD ID | ord-b0de88bf3ad0455f953ed20c84cbbac2 |
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| 出典メモ | uspto-grants-2004_10 |
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