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Condensation of Indoline with Some 1,2-and 1,3-Diketones

机译:吲哚与一些1,2-和1,3-二酮的缩合

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摘要

Bismuth nitrate catalyzed condensation reactions of indoline with 1,2- and 1,3-diketones were investigated and were reported to proceed via different reaction pathways with the involvement of one or two of the carbonyl groups. While the reaction of indoline with cyclohexane-1,3-dione (4) gave solely condensation product, the reaction between the acetylacetone (5) and indoline provided N-acetyl indoline as single products on retro-aldol process. In contrast to 1,3-diketones, the reaction with benzil (17) was performed under difficult conditions and proceeded to give secondary products.
机译:研究了硝酸铋催化的吲哚啉与1,2-和1,3-二酮的缩合反应,并报道其通过不同的反应途径进行,涉及一个或两个羰基。吲哚啉与环己烷-1,3-二酮(4)的反应仅产生缩合产物,而乙酰丙酮(5)和吲哚啉之间的反应在逆醛醇缩合工艺中提供了N-乙酰基吲哚作为单一产物。与1,3-二酮相反,与苯甲腈(17)的反应在困难的条件下进行,并得到副产物。

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