期刊文献+

Environmentally Benign Electrophilic Halogenation of Naphthalenes by H<sub>2</sub>O<sub>2</sub>—Alkali Metal Halides in An Aqueous Cationic Micellar Media

Environmentally Benign Electrophilic Halogenation of Naphthalenes by H<sub>2</sub>O<sub>2</sub>—Alkali Metal Halides in An Aqueous Cationic Micellar Media
下载PDF
导出
摘要 An efficient and greener protocol for the synthesis of 1-halo-naphthols by the action of hydrogen peroxide and alkali metal halides in aqueous micellar media is been described in the present work. This is an environmentally clean and safe procedure, which involved insitu generation of the active halogen in presence of alkali halides. Cationic surfactants such as cetyltrimethylammoniumbromide (CTAB) and cetyltrimethylammoniumchloride (CTAC) were found to facilitate efficiency of halogenation in aqueous media. An efficient and greener protocol for the synthesis of 1-halo-naphthols by the action of hydrogen peroxide and alkali metal halides in aqueous micellar media is been described in the present work. This is an environmentally clean and safe procedure, which involved insitu generation of the active halogen in presence of alkali halides. Cationic surfactants such as cetyltrimethylammoniumbromide (CTAB) and cetyltrimethylammoniumchloride (CTAC) were found to facilitate efficiency of halogenation in aqueous media.
出处 《International Journal of Organic Chemistry》 2012年第3期254-261,共8页 有机化学国际期刊(英文)
关键词 Green Chemistry HALOGENATION Synthesis 1-halo-naphthols Alkali Metal Halides 2-Naphthols AQUEOUS Micellar Media CTAB (Cetyl Trimethyl AMMONIUM Bromide) CTAC (Cetyl Trimethyl AMMONIUM Chloride) Green Chemistry Halogenation Synthesis 1-halo-naphthols Alkali Metal Halides 2-Naphthols Aqueous Micellar Media CTAB (Cetyl Trimethyl Ammonium Bromide) CTAC (Cetyl Trimethyl Ammonium Chloride)
  • 相关文献

参考文献2

二级参考文献24

  • 1Z. G. Le, Z. C. Chen, Y. Hu, Q. G. Zheng,Heterocycles, 2004, 63, 1077.
  • 2Z. G. Le, Z. C. Chen, Y. Hu, Q. G. Zheng, J. Chem. Res.(s),21104. 344.
  • 3General procedure for bromination of phenols: [Bmim]Br3 (1 mmol) was added to phenol (1 mmol) with continuous stirring (reaction conditions see Table 1). After the reaction was completed, the solid crude product was extracted with Et2O, the crude product was directly purified by recrystallization with ethanol/water to give the corresponding pure product of monobromination.
  • 4Z. G. Le, Z. C. Chen, Y.Hu, Q. G. Zheng, Synthesis, 21104, 995.
  • 5K. C. Cannon, G R. Krow, Handbook of Grignard Reagents; Dekker: New York, 1996.
  • 6S.G.Davis, Organotransition Metal Chemistry: Applications to Organic Synthesis;Pergamon Press: Oxford, 1982.
  • 7I.P. Beletskaya, A. V. Cheprakov, Chem. Rev., 2000, 100, 3009 .
  • 8A. Meijere, E E.Meyer, Angew. Chem. Int. Ed. Engl., 1994, 33, 2379.
  • 9W. Cabri, I. Candiani, Acc. Chem.Res., 1995, 28, 2.
  • 10A. Buffer, J. V. Walker, Chem. Rev., 1993, 93, 1937.

共引文献2

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