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.
(Thia)calix[4]arene thiosemicarbazone derivatives 5a and 5b were synthesized by "1 +2" condensation of 1,3-bis[2-(p-formylphenyloxy)ethyloxy]-p-tert-butylcalix[4]arene 4a and 4b with 1-phenylthiosemicarbazide in yields of 84% and 85%, respectively. (Thia)calix[4]arene semicarbazone-bridged derivatives 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.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2009年第8期1278-1281,共4页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No.20402002)
福建省自然科学基金(No.2009J01019)
福建省高校新世纪优秀人才支持计划资助项目
关键词
芳烃
缩氨基脲
合成
桥联
(thia)calix[4]arene
semicarbazone
synthesis
bridging