The peculiarities of the 4-carboxyphenylglyoxal and N-alkoxy-N’-arylureas interaction

Q3 Chemistry
V. G. Shtamburg, V. Shtamburg, A. A. Anishchenko, A. Mazepa
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引用次数: 6

Abstract

It was found that 3-alkoxy-4,5-dihydroxyimidazolidin-2-ones are the only products of interaction of N-alkoxyureas with arylglyoxals which have strong electronegative substituent in the forth position of the aryl moiety. The possibility of obtaining such products as 3-alkoxy-1aryl-5-(4-carboxyphenyl)-4,5-dihydroxyimidazolidin-2-ones, 3-alkoxy-1-alkyl-5-(4-carboxyphenyl)-4,5-dihydroxyimidazolidin-2-ones and 3-alkoxy-1-phenyl-4,5-dihydroxy-5-(4-nitrophenyl)-imidazolidin-2-ones has been verified in the experimental way. In most the cases 3alkoxy-4,5-dihydroxyimidazolidin-2-ones were produced as a mixture of diastereomers.
4-羧基苯乙二醛和n -烷氧基- n ' -芳基脲相互作用的特性
发现3-烷氧基-4,5-二羟基咪唑烷-2-酮是n-烷氧基脲类化合物与芳基乙二醛相互作用的唯一产物,芳基乙二醛在芳基第4位具有强电负性取代基。实验验证了制备3-烷氧基-1芳基-5-(4-羧基苯基)-4,5-二羟基咪唑-2-酮、3-烷氧基-1烷基-5-(4-羧基苯基)-4,5-二羟基咪唑-2-酮和3-烷氧基-1-苯基-4,5-二羟基-5-(4-硝基苯基)-咪唑-2-酮等产物的可能性。在大多数情况下,3烷氧基-4,5-二羟基咪唑烷-2-酮是作为非对映体的混合物产生的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Chemical Bulletin
European Chemical Bulletin Chemistry-Chemistry (all)
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6 weeks
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