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2,6-Dihydroxyanthraquinone → 2,6-Bis(2-morpholinoethoxy)anthraquinone dihydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,6-Dihydroxyanthraquinone | HCID 6776 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Chlorobenzene | HCID 7964 | — |
| 生成物 | 2,6-Bis(2-morpholinoethoxy)anthraquinone dihydrochloride | HCID 20369770 | — |
反応手順
This compound was prepared by the method of Example 3, with the exception that toluene was used as the reaction medium rather than chlorobenzene, from 36 g. (0.15 mole) of 2,6-dihydroxyanthraquinone, 100 g. (0.54 mole) of N-(2-chloroethyl) morpholine hydrochloride, 66g. (1.0 mole) of potassium hydroxide pellets (85%), 400 ml. of toluene and 100 ml. of water. The dihydrocholoride salt was recrystallized twice from isopropanol with enough water added to effect solution. The pure compound melted with decomposition at 288-290° C.; λmax (H2 0) 273 μ, E1cm.1% 778.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04073904 |
| 出典データセット | uspto-grants-1978_02 |
| ORD ID | ord-82cee194515f4adb839daa1a4052b408 |
| 出典メモ | uspto-grants-1978_02 |