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HRID 894477作成日:2026年10月25日

Naphthalene → Anthraquinone

https://huagongshe.com/reaction/894477

反応式

関与物質

役割名称HCID仕込み量
反応物NaphthaleneHCID 931—
反応物TetrahydroanthraquinoneHCID 219295—
生成物AnthraquinoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04284576
出典データセットuspto-grants-1981_08
ORD IDord-a777f0fc97bc4182b784ca51162140ba
出典メモuspto-grants-1981_08