Reaction of N-arenesulfonyl-1,4-benzoquinone imines with acetylacetone
- Authors: Konovalova S.A.1, Avdeenko A.P.1, Lysenko E.N.1, D’yakonenko V.V.2, Shishkina S.V.2
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Affiliations:
- Donbass State Engineering Academy
- Institute for Single Crystals
- Issue: Vol 52, No 4 (2016)
- Pages: 516-522
- Section: Review
- URL: https://bakhtiniada.ru/1070-4280/article/view/214063
- DOI: https://doi.org/10.1134/S1070428016040060
- ID: 214063
Cite item
Abstract
N-Arenesulfonyl-1,4-benzoquinone imines reacted with acetylacetone to afford different products, depending on the isolation procedure. Crystallization from polar protic solvents gave N-[4-hydroxy- 3-(2-hydroxy-4-oxopent-2-en-3-yl)phenyl]arenesulfonamides and 6-(2-oxopropyl)-4-(arenesulfonamido)phenyl acetates, whereas N-(3-acetyl-2,6-dimethyl-1-benzofuran-5-yl)arenesulfonamides were isolated by crystallization from nonpolar aprotic solvents.
About the authors
S. A. Konovalova
Donbass State Engineering Academy
Author for correspondence.
Email: chimist@dgma.donetsk.ua
Ukraine, ul. Shkadinova 72, Kramatorsk, 84313
A. P. Avdeenko
Donbass State Engineering Academy
Email: chimist@dgma.donetsk.ua
Ukraine, ul. Shkadinova 72, Kramatorsk, 84313
E. N. Lysenko
Donbass State Engineering Academy
Email: chimist@dgma.donetsk.ua
Ukraine, ul. Shkadinova 72, Kramatorsk, 84313
V. V. D’yakonenko
Institute for Single Crystals
Email: chimist@dgma.donetsk.ua
Ukraine, pr. Lenina 60, Kharkiv, 61001
S. V. Shishkina
Institute for Single Crystals
Email: chimist@dgma.donetsk.ua
Ukraine, pr. Lenina 60, Kharkiv, 61001
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