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阿魏酰哌嗪盐酸盐的合成
引用本文:肖幼安,黄广,何黎琴,王效山. 阿魏酰哌嗪盐酸盐的合成[J]. 安徽化工, 2011, 37(6): 25-26,30. DOI: 10.3969/j.issn.1008-553X.2011.06.009
作者姓名:肖幼安  黄广  何黎琴  王效山
作者单位:安徽中医学院,安徽省现代中药重点实验室,安徽合肥230031;安徽中医学院,安徽省现代中药重点实验室,安徽合肥230031;安徽中医学院,安徽省现代中药重点实验室,安徽合肥230031;安徽中医学院,安徽省现代中药重点实验室,安徽合肥230031
摘    要:目的:合成阿魏酰哌嗪盐酸盐。方法:以阿魏酸为起始原料,对羟基进行乙酰化保护,得到乙酰阿魏酸,经酰氯化后与哌嗪反应得到单取代哌嗪衍生物,除去乙酰基得到目标物。结果与结论:合成得到了阿魏酰哌嗪,目标化合物通过IR,1HNMR和MS等确证,产率为56.9%。

关 键 词:阿魏酸  哌嗪  阿魏酰哌嗪盐酸盐

Synthesis of 3-(4-Hydroxy-3-methoxy-phenyl)-1 -piperazin-1-yl- propenone Hydrochloride
XIAO You-an,HUANG Guang,HE Li-qin,WANG Xiao-shan. Synthesis of 3-(4-Hydroxy-3-methoxy-phenyl)-1 -piperazin-1-yl- propenone Hydrochloride[J]. Anhui Chemical Industry, 2011, 37(6): 25-26,30. DOI: 10.3969/j.issn.1008-553X.2011.06.009
Authors:XIAO You-an  HUANG Guang  HE Li-qin  WANG Xiao-shan
Affiliation:(Anhui College of Traditional Chinese Medicine,Anhui Modern Traditional Chinese Medicinal Key Laboratory,Hefei 230031,China)
Abstract:Objective:Synthesis of 3-(4-hydroxy-3-methoxy-phenyl)-1-piperazin-1-yl-propenone hydrochloride.Methods:The synthesis involved ferulic acid acetylation protection,then reacted with piperazine to obtain monosubstituted piperazine derivatives,then deacetylase to obtain target product.Results and conclusions:The chemical structure of 3-(4-hydroxy-3-methoxy-phenyl)-1-piperazin-1-yl-propenone hydrochloride was confirmed by IR,1HNMR and MS.The yield was over 56.9%.
Keywords:ferulic acid  piperazine  3-(4-hydroxy-3-methoxy-phenyl)-1-piperazin-1-yl-propenone hydrochloride
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