期刊文献+

3-甲基-1-磺酸咪唑硫酸氢盐催化剂用于四组分一锅法合成不对称聚羟基喹啉衍生物(英文)

Four-component one-pot synthesis of unsymmetrical polyhydroquinoline derivatives using 3-methyl-1-sulfonic acid imidazolium hydrogen sulfate as a catalyst
下载PDF
导出
摘要 3-Methyl-1-sulfonic acid imidazolium hydrogen sulfate has been used as an efficient, halogen-free,and reusable Brnsted acidic ionic liquid catalyst for the synthesis of ethyl-4-aryl/heteryl- hexahydro-trimehtyl-5-oxoquinoline-3-carboxylates via the one-pot condensation of dimedone with aryl/heteryl aldehydes, ethyl acetoacetate, and ammonium acetate under solvent-free conditions. This method has the advantage of being clean and simple, as well as providing the desired product in high yield over a short reaction time. Furthermore, the catalyst could be recycled and reused four times without any discernible reduction in activity. 3-Methyl-1-sulfonic acid imidazolium hydrogen sulfate has been used as an efficient, halogen-free, and reusable Bronsted acidic ionic liquid catalyst for the synthesis of ethyl-4-aryl/heteryl- hexahy-dro-trimehtyl-5-oxoquinoline-3-carboxylates via the one-pot condensation of dimedone with aryl/heteryl aldehydes, ethyl acetoacetate, and ammonium acetate under solvent-free conditions. This method has the advantage of being clean and simple, as well as providing the desired product in high yield over a short reaction time. Furthermore, the catalyst could be recycled and reused four times without any discernible reduction in activity.
出处 《催化学报》 SCIE EI CAS CSCD 北大核心 2014年第7期1036-1042,共7页
关键词 离子液体催化剂 一锅合成 硫酸氢 咪唑 磺酸 四组分 衍生物 不对称 Unsymmetrical polyhydroquinoline Bronsted acidic ionic liquid catalyst Multicomponent reaction Solvent-free condition
  • 相关文献

二级参考文献33

  • 1F.R. Buhlcr, W. Kiowski, J. Hypertcns. 5 (1987) S3.
  • 2A. Sausins, G. Duburs, Heterocycles 7 (1988) 269.
  • 3V. Klusa, Drugs Future 20 (1995) 135.
  • 4M. Li, Z. Zuo, L. Wen, et al. Comb. Chem. 10 (2008) 436.
  • 5S.J. Ji, Z.Q. Jiang, J. Lu, et al. Synlett (2004) 831.
  • 6G. Sabitha, G.S.K. Reddy, C.S. Reddy, et al. Tetrahedron Lett. 44 (2003) 4129.
  • 7M. Maheswara, V. Siddaiah, G.L. Damu, et al. Arkivoc 2 (2006) 201.
  • 8C.S. Re.tidy, M. Raghu, Chin. Chem. Lett. 19 (2008) 775.
  • 9A. Kumar. R.A. Maurya, Tetrahedron Lett. 48 (2007) 388%.
  • 10S.B. Sapkal, K.F. Shelke, B.B. Shingate, et al. Tetrahedron Lett. 50 (2009) 1754.

共引文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部