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磺酸树脂在樟脑肟贝克曼裂解反应中的催化作用 被引量:3

Beckmann Fragmentation of Camphor Oxime Catalyzed by Sulfonic Acid Resin
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摘要 我们发现以磺酸树脂作为固体酸催化樟脑肟贝克曼裂解反应可以生成α-龙脑烯腈.考察了溶剂、催化剂用量、反应温度和反应时间等对反应的影响.在优化条件下樟脑肟可以完全转化,α-龙脑烯腈选择性高达90.5%.动力学研究表明,樟脑肟在磺酸树脂催化下的贝克曼裂解反应服从准一级动力学模型,经过最小二乘法求得反应的表观活化能为64.6kJ/mol. The Beckmann fragmentation of camphor oxime to α-campholenonitrile over solid sulfonic acid resin has been successfully performed. The influences of solvent, reaction temperature and reaction time on the fragmentation were examined. The results indicate that the conversion of oxime can reach 100% with 90.5% of selectivity to α- campholenonitrile under optimal reaction conditions. The kinetics show that Beckmann fragmentation of camphor oxime catalyzed by sulfonic acid resin obeys kinetics rule of the pseudo-first order reaction and the activation energy calculated from least square method is 64.6 kJ/mol.
出处 《分子催化》 EI CAS CSCD 北大核心 2010年第1期25-30,共6页 Journal of Molecular Catalysis(China)
基金 国家自然科学基金项目(No.20572021,20976043)资助
关键词 贝克曼裂解 磺酸树脂 樟脑肟 α-龙脑烯腈 Beckmann fragmentation Sulfonic acid resin Camphor oxime α-Campholenonitrile
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  • 1林森树,符圣和,郑康成,李玉光,詹必增.从α-蒎烯直接催化酯化高选择性地合成乙酸正龙脑酯的研究-催化剂与反应机理初探[J].分子催化,1994,8(1):50-57. 被引量:9
  • 2Giorgio C, Salvatore B. Tetrahedron: Asymmetry [J], 2006, 17 (10), 1 529-1 536;.
  • 3LVShi-jie(吕士杰) WANGLai-lai(王来来).分子催化,1997,11(6):479-483.
  • 4Morita K, Suzuki Z. J. Org. Chem. [J], 1966, 31 (1), 233-237.
  • 5Blaszczyk K, Koenig H, Mel K, et al. Tetrahedron [J], 2006, 62:1 069 -1 078.
  • 6Ernest J B, Cochlaeus H K, et al. CN[P] : 88104903. 4, 1989.
  • 7Stevens R V, Gaeta F C A, Lawrence D S. J. Am. Chem. Soc. [J], 1983, 105 (26) : 7 713 -7 719.
  • 8Hill R K, Mckinnie B G, Conley R T, et al. Tetrahedron [J], 1988, 44 (18) : 3 405 -3 412.
  • 9潘成学,王碧花.龙脑烯腈和龙脑烯酸酯类香料的新合成方法[J].林产化学与工业,2007,27(4):107-110. 被引量:2
  • 10MOHong-bo(莫洪波),YINDu-lin(尹笃林),WANGXiao-guang(王晓光).Master Degree Thesis of Hunan Normal University[D],2004.

二级参考文献49

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  • 1刘福胜,吕清波.杂多酸催化合成2,4,6-三异丙基-1,3,5-三氧恶烷的研究[J].精细化工,1995,12(6):6-8. 被引量:4
  • 2于心玉,刘彩华,彭惠琦,梁学正,杨建国,何鸣元.用离子液体催化合成2,4,6-三异丁基-1,3,5-三氧噁烷[J].合成化学,2006,14(1):88-90. 被引量:3
  • 3陈晓梅,桂建舟,丛晓辉,张晓彤,宋丽娟,孙兆林.功能化酸性离子液体催化异丁醛环化三聚反应[J].石油化工高等学校学报,2005,18(3):30-33. 被引量:4
  • 4潘成学,王碧花.龙脑烯腈和龙脑烯酸酯类香料的新合成方法[J].林产化学与工业,2007,27(4):107-110. 被引量:2
  • 5from Hill R K, Mckinnie B G, Conley R T, et al. Novel products Beckmann Fragmentation of camphor oxime in polyphosphorlc acid [ J ]. Tetrahedron, 1988, 44(18) : 3405-3412.
  • 6Martineza G, Vilaret, Frailea G, et al. Intramolecularactivation evidence for the unexpected Beckmann fragmentation of C (1) - substituted-7-bromonorbomane-2-ones [ J ]. Tetrahedron, 2004, 60 (42) : 9447-9451.
  • 7Yongmei Cui, Eriko Yasutomi, Yuko Otani, et al. Design, synthesis, and characterization of BK channel openers based on oximation of abietane diterpene derivatives [ J ]. Bioorganic & Medicinal Chemistry, 2010,10:8642-8659.
  • 8OGAWA T. Method of preparing 2,4,6 - trisopropopyl - 1, 3,5 - trioxane. JP 53101386 [ P ] : 1978 - 09 - 04.
  • 9AMAGASAKI M F, NAGAOKAKYO T A, SUITA Y S,et al. Method of manufacturing cis, cis - 2,4,6 - trisopropopyl - 1,3,5 - trioxane. US3981889 [ P] : 1976 - 09 - 21.
  • 10华东师范大学.一种制备2,4,6-三异丙基-1,3,5-三氧嗯烷的方法[P].CN1478777A.2004-03-03.

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