期刊文献+

草酸二乙酯与苯酚酯交换反应产物的气相色谱-质谱分析 被引量:1

Analysis of synthesized products from the transesterification of phenol with diethyl oxalate by gas chromatography-mass spectrometry
下载PDF
导出
摘要 采用气相色谱-质谱联用(程序升温)的方法,对MoO3/SiO2催化剂催化草酸二乙酯与苯酚酯交换反应的反应产物进行了分析。结果表明,草酸二乙酯与苯酚酯交换反应生成草酸二苯酯、乙基苯基草酸酯两种反应产物。 The products in the transesterifieation of phenol with diethyl oxalate over MoO3/SiO2 were analyzed by combined means of programmed temperature- capillary gas chromatography - mass spectrometry (GC- MS). The results indicated that the products of transesterification of phenol with diethyl oxalate were diphenyl oxalate and ethyl phenyl oxalate, respectively.
出处 《河北工程大学学报(自然科学版)》 CAS 2009年第1期106-108,共3页 Journal of Hebei University of Engineering:Natural Science Edition
基金 十一五科技支撑计划项目(2006BAE02B00)
关键词 草酸二苯酯 乙基苯基草酸酯 气相色谱-质谱 diphenyl oxalate ethyl phenyl oxalate gas chromatography-mass spectrometry
  • 相关文献

参考文献4

二级参考文献24

  • 1王萍,周志强,叶贵标,王鹏,任红,王秋霞,江树人.高效液相色谱纤维素类手性固定相对外消旋稻丰散的拆分[J].农药,2004,43(12):542-543. 被引量:6
  • 2YASHIMA E, OKAMOTO Y. Chiral discrimination on polysaccharides derivatives[J]. Bulletin of the Chemical Society of Japan, 1995, 68:3 289-3 307.
  • 3WILLIAM L, CHAMPION JR, JAMES LEE, et al. Liquid chromatographic separation of the enantiomers of trans-chlordane, cis-chlordane, heptachlor, heptachlor epoxide and α-hexachlorocyclohexane with application to small-scale preparative separation[J]. J Chromatography A, 2004, 1024: 55-62.
  • 4WAINER I W, ALEMBIK M C, SMITH E. Resolution of enantiomerie amides on a ellulose tribenzoate chiral stationary phase: Mobile phase modifier effects on retention and stero-seleetivity[J]. J Chromatography, 1987, 388: 65-74.
  • 5PIRKLE W H, POCHAPSKY T C. Consideration of chiral recognition relevant to the liquid chromatographic separation of enantiomers[J]. Chemical Review, 1989, 895 347-362.
  • 6MEYER V R, RAIS M. A vivid model of chiral recognition[J]. Chirality,1989, (1) : 167-169.
  • 7Oyevaar, M H, To B W, Doherty M F, et al. Process for Continous Production of Carbonate Esters[P]. US 6093842, 2000.
  • 8Keigo N, Shuji T, Katsumasa H, et al. Process for Producing Diaryl Carbonate[P]. US 5834615, 1998.
  • 9Song H Y, Park E D, Lee J S. Oxidative Carbonylation of Phenol to Diphenyl Carbonate over Supported Palladium Catalysts[J]. J Mol Catal A: Chem , 2000, 154(1~2):243~250.
  • 10Keigo N, Shuji T, Katsumasa H, et al. Process for Producing Polycarbonate[P]. US 5922827, 1999.

共引文献42

同被引文献770

引证文献1

二级引证文献31

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