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(硫杂)杯[4]芳烃缩氨基(硫)脲(桥联)衍生物的合成
引用本文:唐富胜,杨发福,黄智胜,洪碧琼,郭红玉.(硫杂)杯[4]芳烃缩氨基(硫)脲(桥联)衍生物的合成[J].有机化学,2009,29(8):1278-1281.
作者姓名:唐富胜  杨发福  黄智胜  洪碧琼  郭红玉
作者单位:福建师范大学化学与材料学院,福州,350007
基金项目:国家自然科学基金,福建省自然科学基金,福建省高校新世纪优秀人才支持计划资助项目 
摘    要:对叔丁基(硫杂)杯4]芳烃-1,3-二醛基衍生物4a和4b与苯基氨基硫脲进行“1+2”缩合反应, 合成了杯4]芳烃缩氨基硫脲衍生物5a和5b, 产率为84%和85%. 化合物4a和4b与1,6-己基双氨基脲发生“1+1”缩合反应, 合成了杯4]芳烃双缩氨基脲桥联衍生物6a和6b, 产率为83%和80%. 新化合物的结构与构象经元素分析、质谱、核磁共振谱等表征证实.

关 键 词:(硫杂)杯[4]芳烃  缩氨基脲  合成  桥联  
收稿时间:2008-11-8
修稿时间:2008-12-22

Syntheses of (Thia)calix[4]arene (Thio)semicarbazone(-bridged) Derivatives
Tang Fusheng,Yang Fafu,Huang Zhisheng,Hong Biqiong,Guo Hongyu.Syntheses of (Thia)calix[4]arene (Thio)semicarbazone(-bridged) Derivatives[J].Chinese Journal of Organic Chemistry,2009,29(8):1278-1281.
Authors:Tang Fusheng  Yang Fafu  Huang Zhisheng  Hong Biqiong  Guo Hongyu
Institution:(College of Chemistry and Materials, Fujian Normal University, Fuzhou 350007)
Abstract:(Thia)calix4]arene thiosemicarbazone derivatives 5a and 5b were synthesized by “1+2” condensation of 1,3-bis2-(p-formylphenyloxy)ethyloxy]-p-tert-butylcalix4]arene 4a and 4b with 1-phenyl- thiosemicarbazide in yields of 84% and 85%, respectively. (Thia)calix4]arene semicarbazone-bridged de-rivatives 6a and 6b were prepared by reacting compounds 4a and 4b with 1,6-hexylenebis(1-semicarbazide) in “1+1” condensation in yields of 83% and 80%, respectively. The structures and conformations of the new compounds were characterized by elemental analyses, ESI-MS, 1H NMR, etc.
Keywords:(thia)calix[4]arene  semicarbazone  synthesis  bridgi
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