Reaction of N-arenesulfonyl-1,4-benzoquinone imines with acetylacetone


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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.

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S. Konovalova

Donbass State Engineering Academy

编辑信件的主要联系方式.
Email: chimist@dgma.donetsk.ua
乌克兰, ul. Shkadinova 72, Kramatorsk, 84313

A. Avdeenko

Donbass State Engineering Academy

Email: chimist@dgma.donetsk.ua
乌克兰, ul. Shkadinova 72, Kramatorsk, 84313

E. Lysenko

Donbass State Engineering Academy

Email: chimist@dgma.donetsk.ua
乌克兰, ul. Shkadinova 72, Kramatorsk, 84313

V. D’yakonenko

Institute for Single Crystals

Email: chimist@dgma.donetsk.ua
乌克兰, pr. Lenina 60, Kharkiv, 61001

S. Shishkina

Institute for Single Crystals

Email: chimist@dgma.donetsk.ua
乌克兰, pr. Lenina 60, Kharkiv, 61001

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