期刊文献+

Electrochemical Activation of CO_2 for the Synthesis of Ethyl Carbanilate under Mild Conditions 被引量:1

Electrochemical Activation of CO_2 for the Synthesis of Ethyl Carbanilate under Mild Conditions
下载PDF
导出
摘要 A novel electrochemical procedure for the synthesis of ethyl carbanilate from aniline and carbon dioxide was developed via the selective cathodic reduction of carbon dioxide in CO2-saturated DMF solution containing 0. 1 mol/L TEABr at room temperature, followed by the addition of Eft as an alkylating agent. The synthesis was carried outun der mild[p(CO2) = 1.0×10^5 Pa, t =20 ℃ ] and safe conditions. Influences of the nature of the electrodes, the current densities, the passed charges during electrolysis, temperatures, and supporting electrolytes on the yield of ethyl carbanilate were studied to optimize the electrolytic conditions. The selectivity of ethyl carbanilate is 100%. A novel electrochemical procedure for the synthesis of ethyl carbanilate from aniline and carbon dioxide was developed via the selective cathodic reduction of carbon dioxide in CO2-saturated DMF solution containing 0. 1 mol/L TEABr at room temperature, followed by the addition of Eft as an alkylating agent. The synthesis was carried outun der mild[p(CO2) = 1.0×10^5 Pa, t =20 ℃ ] and safe conditions. Influences of the nature of the electrodes, the current densities, the passed charges during electrolysis, temperatures, and supporting electrolytes on the yield of ethyl carbanilate were studied to optimize the electrolytic conditions. The selectivity of ethyl carbanilate is 100%.
出处 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2007年第6期708-711,共4页 高等学校化学研究(英文版)
基金 Supported by the National Natural Science Foundation of China(No.20573037) the Natural Science Foundation of Shang-hai,China(No.05JC1470).
关键词 Carbon dioxide ELECTROCHEMISTRY ANILINE Synthesis Ethyl carbanilate Mild condition Carbon dioxide Electrochemistry Aniline Synthesis Ethyl carbanilate Mild condition
  • 相关文献

参考文献20

  • 1Chaturvedi D. , Kumar M. , Ray S. , Tetrahedron Lett. , 2003, 44, 7637.
  • 2Tascedda P. , Dunach E. , Chem. Comm. , 2000, 449.
  • 3Wan B. S. , Liao S. J. , Yu D. R. , Chem. J. Chinese Universities, 1999, 20(6), 963.
  • 4Chen X. Z. , Hu C. W. , Gao Z. M. , Chem. Res. Chinese Universities, 2005, 21(6), 714.
  • 5KimS. I., ChuF. X., DuenoE. E. , et al. , J. Org. Chem. , 1999, 64, 4578.
  • 6Chen X. Z., Hu C. W., Su J. H. , et al. , Chin. J. Catal. , 2006, 27(6), 485.
  • 7Cassadei M. A. , Moracci F. M. , Zappia G. , J. Org. Chem. , 1997, 62, 6754.
  • 8Feroci M., Cassadei M. A., Orsini M., et al., J. Org. Chem. , 2003, 68, 1548.
  • 9Feroci M. , Inesi A. , Rossi L. , Tetrahedron Lett. , 2000, 41,963.
  • 10Alwis C. D. , Crayston J. A. , Cromie T. , et al. , Electrochim. Acta, 2000, 45, 2061.

同被引文献6

引证文献1

二级引证文献1

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