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4-(5-甲醛基-2-噻吩基)-7-(2-噻吩基)[2,1,3]苯并噻二唑的合成
Synthesis of 4-(5-formyl-2-thienyl)-7-(2-thienyl)[2,1,3]benzothiadiazole
【摘要】 采用两种不同的途径合成了4-(5-甲醛基-2-噻吩基)-7-(2-噻吩基)[2,l,3]苯并噻二唑。研究结果表明,DMF/POCl3体系较n-BuLi/DMF体系产率更高。改变两种合成途径的反应条件,或用单醛化产物进一步醛化,均未发现二醛取代产物的生成。
【Abstract】 4-(5-formyl-2-thienyl)-7-(2-thienyl)[2,1,3]benzothiadiazole(TBT-A) was synthesized through two different synthesis routes. The results shows that the product yield through the route using DMF/POCl3 as reagents is higher than that through the route using n-BuLi/DMF as reagents. The di-formyl substituted product wasn’t produced whether changing the reaction conditions in two synthesis routes or further formaldehydesation using mono-formyl substitute TBT-A.
【关键词】 4-(5-甲醛基-2-噻吩基)-7-(2-噻吩基)[2,1,3]苯并噻二唑;
双醛取代物;
合成;
反应机理;
【Key words】 4-(5-formyl-2-thienyl)-7-(2-thienyl)[2,1,3]benzothiadiazole; di-formyl-substituted product; synthesis; reaction mechanism;
【Key words】 4-(5-formyl-2-thienyl)-7-(2-thienyl)[2,1,3]benzothiadiazole; di-formyl-substituted product; synthesis; reaction mechanism;
【基金】 国家自然科学基金(批准号29974002)资助
- 【文献出处】 天津化工 ,Tianjin Chemical Industry , 编辑部邮箱 ,2007年04期
- 【分类号】TQ252
- 【被引频次】1
- 【下载频次】275