期刊文献+

无溶剂条件下碳基固体酸催化一锅法合成酰胺烷基萘酚(英文) 被引量:1

A facile, green, one-pot synthesis of amidoalkyl naphthols under solvent-free conditions catalyzed by a carbon-based solid acid
下载PDF
导出
摘要 An efficient, environmentally friendly procedure for the synthesis of amidoalkyl naphthols through the one‐pot, three‐component reaction of β‐naphthol, aryl aldehydes, and acetamide in the presence of a carbon‐based solid acid under thermal solvent‐free conditions is described. The beneficial fea-tures of this new synthetic approach include short reaction time, high yields, clean reaction profiles, and a simple work‐up procedure. Furthermore, the catalyst can be readily recycled and reused four times without obvious significant loss of activity. The structure of the catalyst was confirmed by Fourier transform infrared spectroscopy, N2 adsorption/desorption analysis, and X‐ray diffraction. An efficient, environmentally friendly procedure for the synthesis of amidoalkyl naphthols through the one-pot, three-component reaction of β-naphthol, aryl aldehydes, and acetamide in the presence of a carbon-based solid acid under thermal solvent-free conditions is described. The beneficial fea-tures of this new synthetic approach include short reaction time, high yields, clean reaction profiles, and a simple work-up procedure. Furthermore, the catalyst can be readily recycled and reused four times without obvious significant loss of activity. The structure of the catalyst was confirmed by Fourier transform infrared spectroscopy, N2 adsorption/desorption analysis, and X-ray diffraction.
出处 《催化学报》 SCIE EI CAS CSCD 北大核心 2014年第4期490-495,共6页
基金 supported by Islamic Azad University, Mashhad Branch
关键词 一锅法合成 无溶剂条件 固体酸催化 Β-萘酚 胺烷基 碳基 简便 反应时间 Amidoalkyl naphtholCarbon-based solid acidHeterogeneous catalysisSolvent-free condition
  • 相关文献

参考文献6

二级参考文献108

  • 1Tennant, G. In Comprehensive Organic Chemistry, Vol. 1, Eds.: Barton, D.; Ollis, D. W.; Sutherland, I. O., Pergamon, Oxford, 1979, p. 528.
  • 2Fatiadi, A. J. In Preparation and Synthetic Applications of Cyano Compounds, Eds.: Patai, S.; Rappaport, Z., Wiley, New York, 1983.
  • 3Srinivas, K. V. N. S.; Reddy, E. B.; Biswanath, D. Synlett 2002, 625.
  • 4Miller, J. S.; Manson, J. L. Acc. Chem. Rev. 2001, 34, 563.
  • 5Romero, M.; Renard, P.; Caignard, D. H.; Atassi, G.; Solans X.; Constans, P.; Bailly, C.; Pujol, M. D. J. Med. Chem. 2007, 50, 294 and references cited therein.
  • 6Ellis, G. P.; Romney-Alexander, T. M. Chem. Rev. 1987, 87, 779.
  • 7Raja, R.; Adams, R. D.; Blom, D. A.; Pearl, W. C.; Gianotti E. Jr.; Thomas, J. M. Langmuir 2009, 25, 7200.
  • 8Heravi, M. M.; Sadjadi, S.; Hekmatshoar, R.; Oskooie, H A.; Bamoharram, F. F. Chin. J. Chem. 2009, 27, 607.
  • 9Telvekar, V. N.; Akamanchi, K. G. Synth. Commun. 2004, 34, 2331.
  • 10Sarvari, M. H. Synthesis 2005, 787.

共引文献21

同被引文献10

引证文献1

二级引证文献5

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