期刊文献+

HBr催化α-溴代甲基酮类化合物的全脱溴反应研究 被引量:2

Study on the Debromination ofα-Bromomethyl Ketones Catalyzed by HBr
原文传递
导出
摘要 报道了HBr催化下以水为氢源的α-溴代甲基酮类化合物的脱溴化反应.以α-溴代甲基酮类化合物为原料,四氢呋喃为溶剂,α-溴代甲基酮与质量分数5%的氢溴酸的物质的量比为1.0∶0.2时,在180℃下反应5~14 h,分离产率高达94%[高效液相(HPLC)产率96%]的脱溴产物.该方法无金属催化剂参与,催化剂价格低廉,所有产物均经1H NMR和13C NMR结构确证. The debromination reaction ofα-bromomethylketone compounds was achieved by using water as the hydrogen source under the catalysis of HBr.Usingα-bromomethylketones as raw materials,tetrahydrofuran as solvent,when the molar ratio ofα-bromomethylketone to 5%mass fraction hydrobromic acid was 1.0∶0.2,the debrominated product could be obtained with a isolated yield of 94%[high performance liquid chromatography(HPLC)yield 96%]by reacting at 180℃for 5~14 h.All products were confirmed by 1H NMR and 13C NMR spectra.
作者 郑梦霞 曾竟 买里克扎提•买合木提 阿布都热西提•阿布力克木 Zheng Mengxia;Zeng Jing;Meihemuti Mailikezhati;Abulikemu Abudu Rexit(Department of Chemistry,Xinjiang Normal University,Urumqi 830054;School of Chemical Engineering,Xinjiang University,Urumqi 830046)
出处 《有机化学》 SCIE CAS CSCD 北大核心 2021年第5期2121-2126,共6页 Chinese Journal of Organic Chemistry
基金 新疆维吾尔自治区2017年自治区“天山青年计划”(No.2017Q026)资助项目。
关键词 α-溴代甲基酮类化合物 HBR 脱溴 α-bromomethylketone HBr debromination
  • 相关文献

参考文献7

二级参考文献56

  • 1Baudy, R. B.; Greenblatt, L. P.; Jirkovsky, I. L.; Conldin, M.; Russo, R. J.; Bramlett, D. R.; Emrey, T. A.; Simmonds, J. X.; Kowal, D. M.; Stein, R. P.; Tasse, R. P. J. Med. Chem. 1993, 36, 331.
  • 2Seitz, L. E.; Suling, W. J.; Reynolds, R. C. J. Med. Chem. 2002, 45, 5604.
  • 3Kim, Y. B.; Kim, Y. H.; Park, J. Y.; Kim, S. K. Bioorg. Med. Chem. Lett. 2004, 14, 541.
  • 4Hazeldine, S. T.; Polin, L.; Kushner, J.; White, K.; Corbett, T. H.; Biehl, J.; Horwitz, J. P. Bioorg. Med. Chem. 2005, 13, 1069.
  • 5Hazeldine, S. T.; Polin, L.; Kushner, J.; White, K.; Corbett, T. H.; Biehl, J.; Horwitz, J. P. Bioorg. Med. Chem. 2005, 13, 1069.
  • 6Hazeldine, S. T.; Polin, L.; Kushner, J.; White, K.; Corbett, T. H.; Biehl, J.; Horwitz, J. P. Bioorg. Med. Chem. 2005, 13, 3910.
  • 7Hazeldine, S. T.; Polin, L.; Kushner, J.; White, K.; Bouregeois, N. M.; Crantz, B.; Palomino, E.; Corbett, T. H.; Horwitz, J. P. J. Med. Chem. 2002, 45, 3130.
  • 8Hazeldine, S. T.; Polin, L.; Kushner, J.; Paluch, J.; White, K.; Edelstein, M.; Palomino, E.; Corbett, T. H.; Horwitz, J. P. J. Med. Chem. 2001, 44, 1758.
  • 9Rong, F.; Chow, S.; Yan, S.; Larson, G.; Hong, Z.; Wu, J. Bioorg. Med. Chem. Lett. 2007, 17, 1663.
  • 10Hassan, S. Y.; Khattab, S. N.; Bekhit, A. A.; Amer, A. Bioorg. Med. Chem. Lett. 2006, 16, 1753.

共引文献30

同被引文献7

引证文献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