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微波辐射下AlCl_3·6H_2O催化合成β-烯胺酮

AlCl_3·6H_2O catalyzed synthesis of β-enaminones under microwave radiation
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摘要 目的对β-烯胺酮类化合物的微波合成方法的研究。方法在微波辐射下,功率为160W,用AlCl3.6H2O作为催化剂,无溶剂条件下,使乙酰丙酮和1,3-环己二酮分别与一系列胺类化合物反应1~20 min,合成出目标产物。结果合成出的一系列β-烯胺酮类化合物,用红外,1HNMR和元素分析表征了目标化合物的结构;产率为80%~99%。结论该方法具有无溶剂,反应条件温和,操作简单,产率高,反应时间短和产物易分离等优点,是合成β-烯胺酮类化合物的理想方法。 Aim To research the method for microwave-assisted synthesis of β-enaminones.Methods Using AlCl3·6H2O as catalyst,the reaction of acetylacetone or 1,3-dioxocyclohexane and amines was processed under microwave radiation from 1 min to 20 min to give the corresponding β-enaminones under solvent-free condition.Results The structure of the compounds was confirmed by IR,1H NMR and elementary analysis.The yield of the target is 80%~99%.Conclusion The methods were mild,simple and available for synthesis of β-enaminones in good yields without use of solvent.
出处 《西北大学学报(自然科学版)》 CAS CSCD 北大核心 2011年第2期253-257,共5页 Journal of Northwest University(Natural Science Edition)
基金 陕西省教育厅产业化培育基金资助项目(03JC01)
关键词 乙酰丙酮 1 3-环己二酮 β-烯胺酮 AlCl3·6H2O 微波 催化 acetylacetone 1 3-cyclohexanedione β-enaminones AlCl3·6H2O microwave catalysis
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  • 1MICHAEL J P, KONING C B, HOSKEN G D, et al. Reformatskii reactions with N-arylpyrrolidine-2-thiones: synthesis of tricyclic analogues of quinolone antibacterial agents [J]. Tetrahedron,2001, 57(47): 9635-9648.
  • 2AZZARO M, GEPdBALDI S, VIDEAU B. Use of boron trifluoride etherate in the preparation of 2-amino-l-alkenyl ketones from 13-diketones and low-boiling amines[J].Synthesis, 1981,11 : 880-881.
  • 3DANNHARDT G, BAUER A, NOWE U. Non-steroidal anti-inflammatory agents. Part 23. Synthesis and pharma- cological activity of enaminones which inhibit both bovine cyclooxygenase and 5-1ipoxygenase [ J ]. J Prakt Chem, 1998, 340: 256-263.
  • 4BOGER D L, ISHIZAKI T, WYSOCKI J R. et al. Total synthesis and evaluation of (± )-N-( tert-butoxycarbonyl)-CBI, ( ± )-CBI-CDPI1, and (± )-CBI-CDPI2: CC- 1065 functional agents incorporating the equivalent 1, 2, 9, 9a-tetrahydrocyc]opropa [ 1, 2-c] benz [ 1, 2-e] in- dol-4-one ( CBI ) left-hand subunit [ J ]. J Am Chem Soc,1989, 111: 6461-6463.
  • 5CHAABAN I, GREENHILL J V, AKI-ITAR P. Enamino- nes in the mannich reaction. Part 2. Further investiga- tions of internal mannich reactions [ J ]. J Chem Soc,, 1979( 1 ) : 1593-1596.
  • 6ALBEROLA A, CALVO L A, ORTEGA A G, et al. Re- gioselective synthesis of 2 (lh) -pyridinones from fl'amin- oenones and malononitrile, reaction mechanism [ J ]. J Org Chem, 1999, 64(26) : 9493-9498.
  • 7AUGUSTI R, KASCHERES C. Reactions of 3-diazo-1, 3-dihydro-2H-indol-2-one derivatives with enaminones: A novel synthesis of 1, 2, 3-triazoles [ J ]. J Org Chem, 1993, 58(25): 7079-7083.
  • 8EBERLIN M N, KASCHERES C. Catalyzed reaction of diasodiphenylethanone and related diazo ketones with enaminones as a source of pyrmles [ J ]. J Org Chem, 1988, 53 : 2084-2086.
  • 9MULLER A, MAIER A, NEUMANN R, et al. (Alkoxy- carbonyl) carbene transfer to semicyclic enaminones. A route to eyclopenta [b ] pyrrole and indole ring systems [J].Eur J Org Chem,1998,6: 1177-1187.
  • 10MARTIN D F, JANUSONIS G A, MARTIN B B. Stabilities of bivalent metal complexes of some b-ketoimines [J]. J Am Chem Soc,1961, 83: 73-75.

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