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水相中微波辐射下铜催化合成苯并噻唑衍生物
引用本文:柯方,林晨,李鹏.水相中微波辐射下铜催化合成苯并噻唑衍生物[J].福建医科大学学报,2013(5):301-304.
作者姓名:柯方  林晨  李鹏
作者单位:福建医科大学药学院药物化学系,福州350004
基金项目:福建医科大学博士启动基金(2011BS006)
摘    要:目的:用微波辐射催化法在水相中合成苯并噻唑化合物。方法在150 W微波辐射条件下,以CuCl2和菲啰啉为催化剂,2-碘芳烃、芳醛和硫化钠在100℃水相中反应30 min得到目标苯并噻唑化合物。结果合成得到9个相应的苯并噻唑化合物,均通过1 H NMR、13C NMR和质谱确认结构,最高收率为94%。结论使用微波辐射法水相中合成目标产物,与传统方法相比,避免使用大量有机溶剂对环境造

关 键 词:微波辅助合成  苯并噻唑  2-碘芳胺  芳醛  硫化钠

Copper-catalyzed Microwave-assisted Synthesis of Benzothiazoles Derivatives in Water
KE Fang,LIN Chen,LI Peng.Copper-catalyzed Microwave-assisted Synthesis of Benzothiazoles Derivatives in Water[J].Journal of Fujian Medical University,2013(5):301-304.
Authors:KE Fang  LIN Chen  LI Peng
Institution:(Department of Pharmacy, Fujian Medical University, Fuzhou 350004, China)
Abstract:Objective Benzothiazoles were synthesized under microwave irradiation in water . Methods A variety of 2-iodoanilines and aldehydes could be reacted with sodium sulfide to give the desired corresponding products in high yields in 100 ℃ water for 30 min using copper catalysts under microwave ir-radiation . Results We have developed an efficient protocol for benzothiazoles ,9 target compounds can be synthesized in good to excellent yields up to 94% , and all of them were further characterized by 1 H NMR ,13C NMR and MS analysis . Conclusion Synthesis of target benzothiazoles compounds under microwave irradiation in water has an advantage of short reaction time and higher the yields compared to the conventional method .
Keywords:microwave-assisted synthesis  Benzothiazoles  2-Iodoanilines  Aldehydes  Sodium sulfide
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