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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894477Generated: October 25, 2026

Naphthalene → Anthraquinone

https://huagongshe.com/reaction/894477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNaphthaleneHCID 931—
ReactantTetrahydroanthraquinoneHCID 219295—
ProductAnthraquinoneHCID 6780—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284576
Source datasetuspto-grants-1981_08
ORD IDord-a777f0fc97bc4182b784ca51162140ba
Source noteuspto-grants-1981_08