期刊文献+

硼酸催化三组分无溶剂“一锅法””合成5-[(3-吲哚基)-甲基]-2,2-亚丁基-1,3-二噁烷-4,6-二酮衍生物 被引量:5

Solvent-Free One-Pot Three-Component Synthesis of 5-[(Indol-3-yl)-methyl]-2,2-butylidene-1,3-dioxane-4,6-dione Derivatives with B(OH)_3 as Catalyst
原文传递
导出
摘要 在硼酸催化下,以吲哚、醛和2,2-亚丁基-1,3-二噁烷-4,6-二酮为原料,经三组分无溶剂条件合成了9种5-[(3-吲哚基)-甲基]-2,2-亚丁基-1,3-二噁烷-4,6-二酮衍生物.当催化剂的用量为5 mol%时,60℃反应30~90 min,收率为68.6%~91.3%.此外,还探讨了硼酸可能的催化机理.该方法具有反应条件温和,反应时间短且收率高的优点.硼酸催化剂对环境友好且可循环利用. Nine kinds of 5-[(indol-3-yl)-methyl]-2,2-butylidene-l,3-dioxane-4,6-dione derivatives were synthesized by the three-component one-pot reaction of indole with aldehydes and 2,2-butylidene-1,3-dioxane-4,6-dione in the presence of boric acid under solvent-free. The results indicated that the yields ranged from 68.6% to 91.3%, when using 5 mol% boric acid and reacting at 60 ℃for 30~90 min. Furthermore, a proposed reaction mechanism for the reaction catalyzed by boric acidwas speculated. The main advantages of the present procedure were milder conditions, shorter reaction time and higher yields. Further study showed that boric acid was environmentally friendly and reused for six times without any noticeable decrease in the catalytic activity.
出处 《有机化学》 SCIE CAS CSCD 北大核心 2015年第1期212-216,共5页 Chinese Journal of Organic Chemistry
基金 国家科技攻关计划(No.2001BA323C) 江西省研究生创新基金(No.YC10A51)资助项目~~
关键词 三组分反应 一锅法合成 5-[(3-吲哚基)-甲基]-2 2-亚丁基-1 3-二噁烷-4 6-二酮 硼酸催化 three-component reaction one-pot synthesis 5-[(indol-3-yl)-methyl]-2,2-butylidene-1,3-dioxane-4,6-dione B(OH) 3-promoted
  • 相关文献

参考文献6

二级参考文献71

  • 1李小青,杜晓华,徐振元.三氟甲磺酸盐催化甲苯硝化反应的研究[J].有机化学,2006,26(8):1111-1114. 被引量:21
  • 2Sheldon, R. Green Chem. 2000, 2(1), G1.
  • 3Sato, K.; Aokil, M.; Noyori, R. A. Science 1998, 281, 1646.
  • 4Antonelli, E.; D'Aloisio, R.; Gambaro, M.; Fiorani, T.;Venturello, C. J. Org. Chem. 1998, 63, 7190.
  • 5Peng, Y.-Q.; Song, G.-H. World Pestic. 2002, 24(4), 1 (in Chinese).(彭延庆,宋恭华,世界农药,2002,24(4),1.)
  • 6Toda, F. Synlett 1993, 303.
  • 7Tanaka, K.; Toda, F. Chem. Rev. 2000, 100(3), 1025.
  • 8Li, X.-L.; Wang, Y.-M.; Meng, J.-B.; Du, C.-P. Chin.J. Org. Chem. 1998, 18, 20 (in Chinese).(李晓陆,王永梅,孟继本,杜灿屏,有机化学,1998,18,20.)
  • 9Li, X.-L.; Wang, Y.-M. ; Tian, B.; Matuura, T.; Meng, J.B. J. Heterocycl. Chem. 1998, 35, 129.
  • 10Li, X.-L.; Wang, Y.-M.; Matuura, T.; Meng, J.-B. J.Heterocycl. Chem. 1999, 36, 697.

共引文献58

同被引文献52

  • 1刘卉闵,张冬暖,果秀敏,李慧章.超声波辐射下β-吲哚衍生物的合成[J].合成化学,2004,12(5):505-507. 被引量:8
  • 2Wessjohann L A, Rivera D G, Vercillo O E. Muhiple Muhicomponent Macrocyclizations (MiBs) :A Strategic Develoment Toward Macrocycle Diversity[J]. Chem Rev,2009,109(2) :796-814.
  • 3Rovnyak G C, Kimball S D, Benyer B, et al. Calcium Entry Blocks and Activators: Conformational and Structural Deterninants of Dihydropyrinmidine Calcium Channel Modulators [ J ]. J Med Chem, 1995,38 ( 1 ) : 119-129.
  • 4Snider B B,Shi Z. Biomimetic Syntheses of Crambines A, B, C1, and C2 Revision of the Structures of Crambines B and C1 [J]. J Org Chem,1993,58(15) :3828-3839.
  • 5Arimoto H, Hayakawa I, Kuramoto M, et al. Absolute Stereochemistry of Halichtorine: A Potent Inhibitor of VCAM-1 Induction [ J ]. Tetrahedron Lett, 1998,39 ( 8 ) :861-862.
  • 6Makoto K,Chou T,Kaoru Y,et al. Halichlorine, an Inhibitor of VCAM-1 Induction from the Marine Sponge Halichondria Okadai Kadata[ J]. Tetrahedron Lett, 1996,37(22) :3867-3870.
  • 7Dipak P, Debajyoti B, Mukut G, et al. Green Chemsitry Approaches to the Rgioselective Synthesis of Spiro Heterobicyclic Rings Using Iodine as a New and Efficient Catalyst Under Solvent-free Conditions[ J]. Mol Divers ,2011,15:257-261.
  • 8Srinivasa R J, Diya V, Shubha J. NBS/AIBN Promoted One-Pot Multi Component Regioselective Synthesis of Spiro Heterobicyclic Rings via Biginlli-like Condensation Reaction [ J ]. J Chem Pharm Res,2012,4 ( 5 ) :2372 -2379.
  • 9Srinivasa R J, Diya V, Shubha J. Mcrowave-Assisted Synthesis of Spirofused Heterocycles Using Decatungstodivanadogermanic Heteropoly Acid as a Novel and Reusable Heterogeneous Catalyst under Solvent-Free Conditions[ J]. J Cata1,2013,2013 : 1-8.
  • 10Naser M, Khalil P, Masoud B, Soudabeh K. Synthesis of Spiro Heterobicyclic Rings Using Cellulose Sulfuric Acid Under Solvent-Free Conditions[ J]. Asian J Chem,2013,25(6) :3373-3375.

引证文献5

二级引证文献5

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