Knoevenagel冷凝
丙二酸二乙酯
化学
乙酰乙酸乙酯
有机化学
醛
苯甲醛
亚甲基
酮
缩合反应
催化作用
普林斯反应
药物化学
羟醛缩合
出处
期刊:Organic Reactions
日期:2011-03-14
卷期号:: 204-599
被引量:109
标识
DOI:10.1002/0471264180.or015.02
摘要
Abstract Knoevenagel's first papers in this field were concerned with the condensation of formaldehyde with diethyl malonate and with ethyl benzoylacetate. The catalyst was ethylamine. A number of other aldehydes were reported to condense similarly with diethyl malonate, ethyl benzoylacetate, ethyl benzoylpyruvate, and acetylacetone under the influence of various primary and secondary amines. In 1896, Knoevenagel reported benzaldehyde with ethyl aceoacetate condensed at room temperature in the presence of piperdine to give a bis compound, but that when the reaction was run in a freezing mixture, the product was acetoacetate. For the purposes of this chapter, the Knoevenagel condensation is defined as the reaction between an aldehyde or ketone or any compound having an active methylene group, brought about by an organic base or ammonia and their salts.
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