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

被引:2
|
作者
Konovalova, S. A. [1 ]
Avdeenko, A. P. [1 ]
Lysenko, E. N. [1 ]
D'yakonenko, V. V. [2 ]
Shishkina, S. V. [2 ]
机构
[1] Donbass State Engn Acad, Ul Shkadinova 72, UA-84313 Kramatorsk, Ukraine
[2] Natl Acad Ukraine, Inst Single Crystals, Pr Lenina 60, UA-61001 Kharkov, Ukraine
关键词
QUINONE MONOOXIME ESTERS; IMIDES; CHLORINATION; HALOGENATION; BROMINATION; MONOIMINES; RING; IV;
D O I
10.1134/S1070428016040060
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
收藏
页码:516 / 522
页数:7
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