Preparation of Vitamin K3 in Mo–V–P Heteropoly Acid Solutions by Diene Synthesis
The possibility of obtaining vitamin K 3 (2-methyl-1,4-naphthoquinone, menadione) by diene synthesis from accessible substrates such as 2-methylphenol ( o -cresol) and 2-methylaniline ( o -toluidine) was shown. The bifunctional catalysts of these processes are the aqueous solutions of Mo–V–P heterop...
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Veröffentlicht in: | Kinetics and catalysis 2020, Vol.61 (2), p.276-282 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | The possibility of obtaining vitamin K
3
(2-methyl-1,4-naphthoquinone, menadione) by diene synthesis from accessible substrates such as 2-methylphenol (
o
-cresol) and 2-methylaniline (
o
-toluidine) was shown. The bifunctional catalysts of these processes are the aqueous solutions of Mo–V–P heteropoly acids, which allow the oxidation and diene synthesis to be performed as a one-pot process. |
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ISSN: | 0023-1584 1608-3210 |
DOI: | 10.1134/S0023158420010012 |