関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Epichlorohydrin | HCID 7835 | — |
| 反応物 | 2-Hydroxyanthraquinone | HCID 11796 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | 2-[(Oxiran-2-yl)methoxy]anthracene-9,10-dione | HCID 13423601 | 50.57% |
反応手順
112.1 g (0.5 mole) of 2-hydroxyanthraquinone are dissolved in 500 ml of N-methylpyrrolidone, and 12 g (0.5 mole) of sodium hydride are added in portions. When the evolution of gas has ended, 46.37 ml (0.5 mole) of epichlorohydrin are added dropwise at 70° C. and stirring is continued at 70° C. for a further 8 hours. 1.5 liters of water are then added, the mixture is filtered and the filter cake is dried in vacuo. After drying, the product is boiled up again in 1 liter of N,N-dimethylformamide with 10 g of active charcoal and filtered hot. The crystals which precipitate on cooling to 0° C. are separated off by filtration and dried under a high vacuum. 69.45 g (50.57% of theory) of 2-anthraquinonyl glycidyl ether are obtained;
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04849533 |
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| 出典データセット | uspto-grants-1989_07 |
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| ORD ID | ord-c5fe9765ef3445faa73491c8e34e0c63 |
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| 出典メモ | uspto-grants-1989_07 |
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