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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971827Generated: October 26, 2026

1,3-Butadiene → Tetrahydroanthraquinone

https://huagongshe.com/reaction/971827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-ButadieneHCID 7845—
Reactant1,4-NaphthoquinoneHCID 8530—
ProductTetrahydroanthraquinoneHCID 219295—

Reaction Steps

A process has now been found for the isolation of purified anthraquinone from the crude anthraquinone which has been obtained by oxidation of naphthalene to give naphthoquinone, reaction of the oxidation product with butadiene to give tetrahydroanthraquinone, oxy-dehydrogenation of this reaction product with molecular oxygen to give a crude anthraquinone and optionally removal of naphthalene, phthalic anhydride and low-boiling substances from this crude anthraquinone, which is characterised in that the crude anthraquinone is treated with an oxygen compound of the elements of the first and/or second main group of the periodic system at an elevated temperature, optionally in the presence of a solvent, and purified anthraquinone is then isolated by subliming the anthraquinone present at a temperature of about 190° to about 290° C. and a pressure of about 1 to about 90 mm Hg and then desubliming it under the same pressure, or by vaporising the pretreated anthraquinone at a temperature of about 290° to about 380° C. and a pressure of about 90 to about 760 mm Hg and condensing the vapour under a pressure of about 90 to about 760 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04161481
Source datasetuspto-grants-1979_07
ORD IDord-fbb6590268f240f68f025fa44b273537
Source noteuspto-grants-1979_07