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作 者:石秀梅[1] 邓士英[1] 邹桂华[1] 岳司佳[1]
机构地区:[1]牡丹江医学院药学系,黑龙江牡丹江157011
出 处:《化学工程师》2008年第6期8-9,共2页Chemical Engineer
基 金:黑龙江省卫生厅科研课题(2003-152);黑龙江省教育科学规划课题(738)
摘 要:探索黄酮类化合物的合成方法。采用一种新方法,通过酰基化、Fries重排、醇醛缩合反应,合成了3,5-二羟基查尔酮,获得了满意的收率(80%)。该方法具有反应时间短、操作简便、收率高等优点。The synthetic methods of flavonoids were studied. Synthesis of 3,5 -dihydroxy chalcone was accomplished by acylation, Fries rearrange reaction and aldol condensation. 3,5 - Dihydroxy chalcone was synthesize and a good yield(80% ) was obtained. This method is charactered by the reaction time being short,the operation process being simple and the yield being good.
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