期刊文献+

液-液相转移催化Wittig-Horner反应合成二苯乙烯 被引量:2

Synthesis of Stilbene by Wittig-Horner Reaction with L-L PTC
下载PDF
导出
摘要 针对当前二苯乙烯的合成工艺存在反应时间长、收率低、产品分离成本高等问题,提出了液-液相转移催化合成二苯乙烯的新方法。详细研究了各种因素如搅拌速率、催化剂种类与用量、有机溶剂种类与体积、氢氧化钠浓度和温度对相转移催化反应体系的影响,并探讨了液-液相转移催化反应机理。以用量为6%的四丁基溴化铵作催化剂,在甲苯/50%的烧碱溶液体系中于45℃、1 200 r/分钟下反应80分钟,苯甲醛的转化率为92.6%,并且反应产物全为E式构象。研究结果表明:液-液相转移催化Wittig-Horner反应为萃取机理,这为二苯乙烯母体结构化合物的绿色工业化生产提供了新的合成路径。 To counter problems such as long reaction time, low yield, high cost of separating product and so on, a novel synthetic method of liquid-liquid phase transfer catalysis ( L-L PTC) for synthesizing stilbene was presented. The effects of agitation speed, kinds and amounts of catalysts, kinds and volumes of organic solvents, concentration of NaOH and temperature on catalysis reaction were investigated in detail, and a mechanism of Wittig-Horner reaction was given. The conversion of benzaldehyde could reach 92.6% when dosage of catalyst tetra-n-butylammonium bromine (TBAB) was 6%, reaction at 45 ℃ with 1200 rpm for 80 minutes in a toluene / aqueous NaOH (wt 50% ) system; all product were E-alkenes. The results showed that reaction of L-L PTC was Starks extraction mechanism rather than Makosza interfacial mechanism. The study provided a new synthetic method for green industrial production of stilbenoid.
出处 《染料与染色》 CAS 2013年第5期41-46,共6页 Dyestuffs and Coloration
关键词 液-液相转移催化 WITTIG-HORNER反应 萃取机理 二苯乙烯 liquid-liquid phase transfer catalysis Wittig-Horner reaction extraction mechanism stilbene
  • 相关文献

参考文献14

  • 1Starks C M, Liotta C L, Halpern M. Phase - transfer catalysis: fundamentals, applications and industrial perspectives [ M ]. 1st ed. New York: Chapman & Hall, 1994:1 -22. 被引量:1
  • 2何瑾馨..染料化学[M],2004.
  • 3葛广周,缪永祥.Wittig反应及其改良法在荧光增白剂合成中的应用[J].印染助剂,2006,23(8):10-14. 被引量:4
  • 4尹志刚主编..有机磷化合物[M].北京:化学工业出版社,2011:319.
  • 5Heck R F, Nolley J P. Palladium - catalyzed vinylic hydrogen sub- stitution reactions with aryl, benzyl, and styryl halides [ J ]. J. Org. Chem., 1972, 37 (14): 2320-2322. 被引量:1
  • 6Imad A. Synthesis of biphenols containing anhydride, imido or dicy- ano arylene moieties [ J ]. Synthetic Communications, 1999, 29 (17) : 2915 -2922. 被引量:1
  • 7Stalmach U, Detert H. Synthesis and electronics spectra of substitu- ted p - distyrylbenzenes for the use in light - emitting diodes [ J ]. J. Prakt. Chem., 2000, 342 (1): 10-16. 被引量:1
  • 8Wang M L, Rajendran V. Kinetics for dichlorocyclopropanation of 1, 7 - octadiene under the in? uence of ultrasound assisted phase - transfer catalysis conditions [ J ]. J. Mol. Catal. A: Chem., 2007, 273:5 -13. 被引量:1
  • 9Landini D, Maia A, Rampoldi A. Extractability and reactivity of OH - in low polarity media under phase - transfer conditions: dra- matic effect of the aqueous base concentration [ J ]. J. Org. Chem., 1986, 51:5476-5478. 被引量:1
  • 10Kenjo T, Diamond R M. Hydration of the halide ions in certain or- ganic solvents [ J]. J. Ianrg. Nucl. Chem., 1974, 36:183 -188. 被引量:1

二级参考文献23

共引文献3

同被引文献13

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