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Hydrochloric Acid → 9,10-Anthracenedione, 2,3-dihydro-1,4,5,8-tetrahydroxy-
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1,5-Diamino-4,8-dihydroxyanthraquinone | HCID 67351 | — |
| 反応物 | Sodium Bisulfite | HCID 23665763 | — |
| 生成物 | 9,10-Anthracenedione, 2,3-dihydro-1,4,5,8-tetrahydroxy- | HCID 66485 | — |
反応手順
To crude 1,5-diamino-4,8-dihydroxyanthraquinone (11 g, 0.041 mol) was added NaOH (2.5 M, 200 mL) and the suspension was refluxed gently for 3 hours before it was allowed to cool down to room temperature. Sodium hydrogen sulphite (31.74 g, 0.182 mol) was added portionwise and the reaction mixture was refluxed again for 3 hours. It was cooled down to room temperature and was acidified with concentrated hydrochloric acid until pH 3. The precipitate was isolated by filtration and washed successively with cold water and then hot water. After lyophilisation overnight, the title compound was afforded as a crude brown solid (8 g, 73%). FAB MS, m/z(M+H)+ 251.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07557215B2 |
| 出典データセット | uspto-grants-2009_07 |
| ORD ID | ord-bfbc5450904d47cd921314288f591e6c |
| 出典メモ | uspto-grants-2009_07 |