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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >ACETOXYLATION OF 6,7-DIALKOXY-SUBSTITUTED 1,4-DIHYDROQUINOXALINE-2,3-DIONES (QXS) USING FUMING NITRIC ACID IN ACETIC ACID - A FACILE SYNTHESIS OF 5-ACYLOXY-6,7-DIALKOXY QXS
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ACETOXYLATION OF 6,7-DIALKOXY-SUBSTITUTED 1,4-DIHYDROQUINOXALINE-2,3-DIONES (QXS) USING FUMING NITRIC ACID IN ACETIC ACID - A FACILE SYNTHESIS OF 5-ACYLOXY-6,7-DIALKOXY QXS

机译:在乙酸中使用冒烟的硝酸乙酰化6,7-二甲氧基取代的1,4-二羟基喹喔啉-2,3-二酮(QXS)-轻松合成5-乙酰基-6,7-二甲氧基QXS

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摘要

Treatment of 6,7-dialkoxy-1,4-dihydroquinoxaline-2,3-diones 3 with fuming nitric acid in acetic acid at 25 degrees C resulted in an acetoxylation reaction, giving 5-acetoxy-6,7-dialkoxy-1,4-dihydroquinoxaline-2,3-diones 4 in moderate yields. A mechanism involving ipso attack of nitronium ion as the first step is proposed. [References: 14]
机译:在25°C下用发烟硝酸在乙酸中处理6,7-二烷氧基-1,4-二氢喹喔啉-2,3-二酮3进行乙酰氧基化反应,得到5-乙酰氧基-6,7-二烷氧基-1, 4-二氢喹喔啉-2,3-二酮4的产率中等。第一步,提出了涉及硝基离子的ipso攻击的机理。 [参考:14]

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