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One-Pot Process for Preparing Substituted Anthraquinones via Diene Synthesis in the Presence of Solutions of Mo-V-P Heteropoly Acids Full article

Journal Catalysis in Industry
ISSN: 2070-0504 , E-ISSN: 2070-0555
Output data Year: 2014, Volume: 6, Number: 4, Pages: 273-277 Pages count : 5 DOI: 10.1134/S2070050414040096
Tags Anthraquinones, Diene synthesis, Heteropoly acids
Authors Gogin L.L. 1 , Zhizhina E.G. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090 Russia

Abstract: The acid catalyzed condensation of substituted 1,3-butadienes with para-quinones and the oxidation of the resulting adducts can be conducted as one operation using aqueous solutions of Mo-V-P heteropoly acids (HPAs) of the general composition H a P z Mo y V x O b . Being strong Brønsted acids and at the same time reverse oxidizers, these solutions have bifunctional catalytic properties. The condensation of 1,4-naphthoquinone (NQ) with 1,3-butadiene in solutions of high-vanadium HPAs with the molecular formulas H15P4Mo18V7O89 and H17P3Mo16V10O89 using a water-miscible organic solvents (acetone and 1,4-dioxane) gives 9,10-anthraquinone (AQ) with yields of 70% and purities of up to 97% upon the complete conversion of NQ. The reaction between NQ and substituted 1,3-butadienes under similar conditions allows us to obtain substituted anthraquinones with yields of up to 90% and purities of up to 99%. The catalysts are regenerated with oxygen in a separate stage and used multiple times.
Cite: Gogin L.L. , Zhizhina E.G.
One-Pot Process for Preparing Substituted Anthraquinones via Diene Synthesis in the Presence of Solutions of Mo-V-P Heteropoly Acids
Catalysis in Industry. 2014. V.6. N4. P.273-277. DOI: 10.1134/S2070050414040096 WOS Scopus РИНЦ OpenAlex
Original: Гогин Л.Л. , Жижина Е.Г.
One-Pot процесс получения замещенных антрахинонов диеновым синтезам в присутствии растворов Mo-V-P гетерополикислот
Катализ в промышленности. 2014. №4. С.33-38. РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jan 28, 2014
Published print: Oct 1, 2014
Published online: Dec 24, 2014
Identifiers:
Web of science: WOS:000433673400004
Scopus: 2-s2.0-84919983446
Elibrary: 24026270
OpenAlex: W2087406344
Citing:
DB Citing
Scopus 4
Elibrary 5
OpenAlex 2
Web of science 5
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