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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 971827Erstellt: 23. Oktober 2026

1,3-Butadiene → Tetrahydroanthraquinone

https://huagongshe.com/de/reaction/971827

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,3-ButadieneHCID 7845—
Edukt1,4-NaphthoquinoneHCID 8530—
ProduktTetrahydroanthraquinoneHCID 219295—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04161481
Quelldatensatzuspto-grants-1979_07
ORD IDord-fbb6590268f240f68f025fa44b273537
Quellennotizuspto-grants-1979_07