期刊文献+

超声波促进新型席夫碱类化合物的水相合成

Ultrasound-assisted Synthesis of Novel Schiff Bases in Aqueous Condition
下载PDF
导出
摘要 在超声波促进下以聚乙二醇(PEG 6000)为相转移催化剂,在水相中合成了8个席夫碱类化合物。采用1HNMR、13CNMR、IR、MS(ESI)和X-射线衍射对其结构进行了表征,结果与目标化合物一致。采用相转移催化剂水相超声波合成,与传统的加热反应或有机溶剂相超声波合成比较,水相超声波合成不但可以避免使用酸碱催化剂和乙醇等挥发性溶剂,而且使得反应时间从数小时缩短至0.5 h左右,产率高达76%~92%。经查证,其中6个席夫碱类化合物是未见文献报道的新化合物。 Eight Schiff bases were synthesized by aqueous phase with polyethylene glycol(PEG 6000) as phase transfer catalyst under ultrasonic radiation.The structures were confirmed by 1HNMR,13CNMR,IR,MS(ESI) and X-ray and were consistent with the target compounds.Compared with the traditional heating reaction or the organic solvent phase ultrasonic synthesis,the aqueous phase ultrasonic synthesis with phase transfer catalyst could not only avoid the volatile solvents such as acid-base catalyst and ethanol,but also shorten the reaction time from several hours to about 0.5 h,and the yield was as high as 76% to 92%.It was verified that six Schiff bases were new compounds which were not reported in the literature.
作者 邓仰平 高旭 谢晓蓉 蒋小强 王世范 DENG Yang-ping;GAO Xu;XIE Xiao-rong;JIANG Xiao-qiang;WANG Shi-fan(Key Laboratory of Tropical Biological Resources of the Ministry of Education,Department of Phar-macy,School of Life and Pharmaceutical Sciences,Hainan University,Haikou 570228,China)
出处 《化学试剂》 CAS 北大核心 2020年第3期321-325,共5页 Chemical Reagents
基金 海南省自然科学基金资助项目(218MS005)。
关键词 PEG 6000 超声辅助 相转移催化剂 席夫碱 水相合成 PEG 6000 ultrasonic radiation phase tranfer catalyst Schiff bases aqueous-phase synthesis
  • 相关文献

参考文献2

二级参考文献24

  • 1边延江,赵艳军,栗明献,李记太.超声波辐射下金属锰引发芳香醛的偶联反应[J].有机化学,2004,24(7):828-830. 被引量:12
  • 2张珉,李毅群,罗慧谋,周美云.离子液体促进四氟硼酸铜催化芳醛和乙酸酐合成1,1-二乙酸酯[J].有机化学,2005,25(7):842-845. 被引量:8
  • 3Nimitsiriwat N, Marshall E. L, Gibson, et. al. Unprecedented Reversible Migration of Amide to Sehiff Base Ligands Attached to Tin: Latent Single L Site Initiators for Laetide Polymerization[J ]. J. Am. Chem. Soc, 2004,126(42) : 13598 - 13599.
  • 4Shibata, M. Tanirnoto, T. Kandori, et. al. Molecules in the Sehiff Base Region of Bacteriorhodopsin[ J ]. J. Am. Chem. Soc, 2003, 125(44) : 13312 - 13313.
  • 5Okino T, Takemoto Y. Asymmetric Alkylation of tert - Butyl Gtycinate Schiff Ease with Chiral Quaternary Ammonium Salt under Micellar Conditions[J]. Org. Lett. 2001,3(10) : 1515 - 1517.
  • 6Hajipour A R,Mohammadpcor-Baltork I,Bigdeli M. A Convenient and Mild Procedure for theSynthesis of Hydrazones and Semicarbazones from Aldehydes or Ketones under Solvent - free Condition[J]. J. Chem. Research (8),1999,9:570- 571.
  • 7Welton T. Room - Temperature Ionic Liquids. Solvents for Synthesis and Catalysis [J ]. Chem. Rev, 1999, 99:2071 - 2084.
  • 8Holbrey J D Sedden K R. The Phase Behaviour of 1 - alkyl - 3 - methylimidszolium Tetrafluoroborates: Ionic Liquids and Ionic Liquid Crystals[J]. J. Chem. Soc Dalton Trans. 1999: 2133--2139.
  • 9Kiasat A R Kazemi, F. Mehrjardi, et al. Synthesis of Semicarbazones From Carbonyl Compounds Under Solvent Free Conditions[J ]. Asian J. Chem. 2005,17(4) :2830 - 2832.
  • 10Hania M M. Synthesis and Antibacterial Activity of Oximes. Semicarbazones and Phenylhydramnes. Asian [J ]. J. Chem. 2005,17(1 ) :439--442.

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