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Synthesis of 1,4-Dimethyl-9,10-Anthraquinone from 1,4-Naphthoquinone and 2,4-Hexadiene in the Presence of Heteropoly Acids Full article

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 2019, Volume: 60, Number: 1, Pages: 69-73 Pages count : 5 DOI: 10.1134/s0023158419010087
Tags anthraquinones; diene synthesis; high-vanadium heteropoly acids
Authors Gogin L.L. 1 , Zhizhina E.G. 1 , Pai Z.P. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090 Russia

Funding (1)

1 Federal Agency for Scientific Organizations 0303-2016-0008

Abstract: The synthesis of 1,4-dimethyl-9,10-anthraquinone (DMAQ) from 1,4-naphthoquinone and 2,4‑hexadiene was studied based on a new one-step method developed by the authors for the synthesis of substituted anthraquinones. A solution of high-vanadium heteropoly acid with the empirical formula H17P3Mo16V10O89 (HPA-10) was used as a bifunctional (acid and oxidation) catalyst. It was found that a reaction with 2,4-hexadiene, unlike other methylbutadienes, does not proceed so smoothly, and it leads to the formation of a mixture of DMAQ, its dihydro derivative, and tarry products. Possible reasons for the results obtained are discussed.
Cite: Gogin L.L. , Zhizhina E.G. , Pai Z.P.
Synthesis of 1,4-Dimethyl-9,10-Anthraquinone from 1,4-Naphthoquinone and 2,4-Hexadiene in the Presence of Heteropoly Acids
Kinetics and Catalysis. 2019. V.60. N1. P.69-73. DOI: 10.1134/s0023158419010087 WOS Scopus РИНЦ ANCAN OpenAlex
Original: Гогин Л.Л. , Жижина Е.Г. , Пай З.П.
Синтез 1,4-диметил-9,10-антрахинона из 1,4-нафтохинона и 2,4-гексадиена в присутствии гетерополикислот
Кинетика и катализ. 2019. Т.60. №1. С.75-80. DOI: 10.1134/s045388111901009xRSCI РИНЦ OpenAlex
Dates:
Submitted: Jun 27, 2018
Accepted: Aug 13, 2018
Published print: Jan 1, 2019
Published online: May 15, 2019
Identifiers:
Web of science: WOS:000468063400009
Scopus: 2-s2.0-85066042843
Elibrary: 41657980
Chemical Abstracts: 2019:964965
Chemical Abstracts (print): 171:61573
OpenAlex: W2946808818
Citing:
DB Citing
Scopus 7
Web of science 6
Elibrary 6
OpenAlex 6
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