摘要
用丁二酰氯作为酰化试剂合成了五个芳香族1,4—二酮(3a—3e),产率较文献报道的有较大提高.同时用丁二酸酐作为酰化试剂也合成得到了3a.前法可用于制备1,4位含相同芳基的1,4—二酮,而后法则可用于1,4位含不同芳基的1,4—二酮的合成.
Five aromatic 1,4—diketones(3a—3e)were prepared by modifiedmethod using succinyl chloride as acylating reagent.The yield of the 1,4—diketones was much higher than the yield with the literature method.Aromatic 1,4—diketone(3a)was also prepared by using succinic anhydrideas acylating reagent.The first method could be used for the preparationof aromatic 1,4—diketones with the same aromatic groups,and the secondfor the different aromatic groups.
出处
《兰州大学学报(自然科学版)》
CAS
CSCD
北大核心
1989年第3期60-63,共4页
Journal of Lanzhou University(Natural Sciences)
基金
国家自然科学基金
关键词
双黄酮
化合物
合成
付氏反应
Synthesis
Biflavonoid
Aromatic 1, 4—diketone
Friedel—Crafts reaction