摘要
末端炔烃是有机合成中重要的原料或中间体.通过钯催化的Sonogashira偶联反应,将2-甲基-3-丁炔-2-醇连接到其它基团上所得到的结构,可以看作是一类丙酮保护的末端炔烃.目前,对于这种丙酮保护的末端炔烃,其去保护得到端基炔主要是通过KOH存在下在甲苯中回流数小时的方法,但是反应温度高,条件苛刻,适用范围较窄.对这一脱保护过程进行研究,通过对多种溶剂和反应温度进行对比,发现以1,4-二氧六环作为溶剂,KOH作为碱,可以在相对较低的温度(60℃)下得到较高的产率,而且所需时间大大缩短(0.5~2 h),拓展了这种方法的应用范围.
Terminal alkynes are important building blocks in organic synthesis. Acetone protected terminal alkynes are frequently used in alkyne synthesis and reactions, which could be easily prepared by Pd-catalyzed Sonogashira cross-coupling reactions between electrophiles and 2-methyl-3-butyn-2-ol. At present, the deprotection of the acetone protected terminal alkynes is generally carried out in reflux toluene in the presence of potassium hydroxide for hours. However, this procedure suffers from the harsh reaction conditions and its application has been limited. Here in the deprotection of acetones has been discussed, and various solvent, temperature, substrates were investigated to advance the procedure, and it is found that by employing 1,4-dioxane as solvent, this process can undergo smoothly at 60℃ with satisfying yields in 0.5~2 h in the presence of 2.0 equiv. KOH.
作者
关志朋
师瑶
石炜
陈浩
Guan Zhipeng Shi Yao Shi Wei Chen Hao(College of Science, Huazhong Agricultural University, Wuhan 43007)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2017年第2期418-422,共5页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No.21202050)
湖北省自然科学基金(No.2014CFB930)资助项目~~
