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Naphthalene → Anthraquinone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Naphthalene | HCID 931 | — |
| 反応物 | Tetrahydroanthraquinone | HCID 219295 | — |
| 生成物 | Anthraquinone | HCID 6780 | — |
反応手順
In the process according to U.S. Pat. No. 2,938,913, the mixture which is present after the Diels-Alder reaction and which contains tetrahydroanthraquinone, solvent and naphthalene is first treated with aqueous alkali, an aqueous alkaline solution of salts of tetrahydroanthraquinone and a mixture of solvent and naphthalene being obtained. Crude solid anthraquinone is isolated from the solution containing the salts of tetrahydroanthraquinone by passing air through this solution and filtering off the anthraquinone which precipitates out. The mixture of naphthalene and the solvent is separated, by distillation, into the components, which can then be re-used in the anthraquinone synthesis.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04284576 |
| 出典データセット | uspto-grants-1981_08 |
| ORD ID | ord-a777f0fc97bc4182b784ca51162140ba |
| 出典メモ | uspto-grants-1981_08 |