期刊文献+

5-溴-2-甲氧基苯酚的合成

Synthesis of 5-Bromo-2-Methoxyphenol
下载PDF
导出
摘要 5-溴-2-甲氧基苯酚是一种重要的农药、医药中间体,本文以邻甲氧基苯酚为原料,乙酰化、溴化、脱保护得到5-溴-2-甲氧基苯酚,总收率为64.3%,产物的结构通过1HNMR、13CNMR及元素分析进行验证。 5-bromo-2-methoxyphenol was synthesized from guaiacol via protection of phenolic hydroxyl group, bromination with bromine, and deprotection, with the overall yield of 64.3%. The structure of the product was confirmed by 1HNMR, 13CNMR and elementary analysis.
出处 《浙江化工》 CAS 2011年第10期6-8,共3页 Zhejiang Chemical Industry
基金 浙江省重点科技创新团队项目(2011R09028-10)
关键词 邻甲氧基苯酚 溴化 5-溴-2-甲氧基苯酚 脱保护 guaiacol bromination 5-bromo-2-methoxyphenol deprotection
  • 相关文献

参考文献9

  • 1钟嫄,罗利,赵桂森.阿利克仑合成路线图解[J].中国医药工业杂志,2009,40(6):468-473. 被引量:3
  • 2Tsou E L, Chen S Y, Yang M H, et al. Synthesis and biological evaluation of a 2-aryl polyhydroxylated py,Tolidine alkaloid-based library [J]. Bioorg. Med. Chem., 2008, 16(24): 10198-10204.
  • 3Alejandro C D. Kumada-cm-riu cross coupliug route to the anti-cancer agent combretastatin A-4 [J]. Synth. Commun., 2008, 38(21): 3823-3833.
  • 4Fujikawa N, Ohta T, Yamaguchi T, et al. Total synthesis of lamellarins D, L, and N [J].Tetrahedron, 2006, 62 (4): 594-604.
  • 5Nobuhito K, Tomio I, Masao T. Facile preparation of organozinc bromides using electrogenerated highly reactive zinc and its use in cross-coupling reaction [J]. Tetrahedron, 2005, 61(47): 11125-11131.
  • 6Quideau S, Fabre I, Deffieux D. First asymmetric synthesis of orthoquinone monoketal enantiomers via anodic oxidation [J]. Org. Lett., 2004, 6(24): 4571-4573.
  • 7Vandermey M, Hatzelmann A, Vanklink G P M, et al. Novel selective PDE4 inhibitors. 2. Synthesis and structure- activity relationships of 4-aryl-substiluted cis-tetra- and eishexahydrophthalazinones [J]. J. Med. Chem., 2001, 44 (16): 2523-2535.
  • 8David B S, Corey E J. A two-step total synthesis of the natural pentacyele tlichodimerol, a novel inhibitor of TNF-a production [J]. J. Org. Chem., 2004, 69(25): 8731-8738.
  • 9Pinney K G, Sriram M. Combretastatin analogs with tubulin binding activity: W0,2006138427[P]. 2006-11-28.

二级参考文献28

  • 1Mickel SJ. Alternative synthesis of aryl-octanoyl amide compounds: GB, 2431654 [P]. 2007-05-02. (CA 2007, 146: 461957)
  • 2Sedelmeier G. Alternative synthesis of aryl-octanoyl amide compounds: GB, 2431646 ~P]. 2007-05-02. (CA 2007, 146: 461958)
  • 3Mickel SJ. Alternative synthesis of aryl-octanoyl amide compounds: GB, 2431653 [P]. 2007-05-02. (CA 2007, 146: 461962)
  • 4Sedelmeier G. Synthesis of aryl-octanoyl amide compounds: GB, 2431647 [P]. 2007-05-02. (CA 2007, 146:481827)
  • 5Marterer W. Alternative synthesis of aryl-octanoyl amide compounds: GB, 2431649 [P]. 2007-05-02. (CA 2007, 146: 461961)
  • 6Marterer W. Alternative synthesis of aryl-octanoyl amide compounds: GB, 2431640 [P]. 2007-05-02. (CA 2007, 146: 461964)
  • 7Marterer W. Synthesis of aryl-octanoyl amide compounds: GB, 2431644 [P]. 2007-05-02. (CA 2007, 146: 461959)
  • 8Mickel SJ. Alternative synthesis of aryl-octanoyl amide compounds: GB, 2431641 [P]. 2007-05-02. (CA 2007, 146: 461967)
  • 9Mickel SJ. Alternative synthesis of aryl-octanoyl amide compounds: GB, 2431642 [P]. 2007-05-02. (CA 2007, 146: 461966)
  • 10Acemoglu M. Alternative synthesis of aryl-octanoyl amide compounds: GB, 2431648 [P]. 2007-05-02. (CA 2007, 146: 481829)

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