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-Dibutyl-3-aminophenol | HCID 601234 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Anthraquinone | HCID 6780 | — |
反応手順
One part by weight of 1-amino-2-chloro-4-hydroxyanthraquinone, 10 parts by weight of 1,3-dimethyl-2-imidazolidinone, 1.0 part by weight of potassium carbonate and 1.0 part by weight of N,N-di-n-butyl-m-aminophenol were mixed at room temperature, and then heated to 140° C. While this temperature was maintained, the reaction was conducted for 3 hours. The reaction mixture was then cooled to room temperature, charged into 90 parts by weight of water, and extracted with toluene. After the solution was separated, toluene was distilled off under reduced pressure, and the residue was purified through silica gel column chromatography to obtain an anthraquinone compound as coloring matter No. 9 (yield 90%) in Table 1.
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-3e59d5b30b05441bb33a290e341e3ebc |
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| 出典メモ | uspto-grants-2004_10 |
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