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羧酸和酯类化合物在Friedel-Crafts反应中的应用 被引量:1

Application of Carboxylic Acids and Esters to Friedel-Crafts Reactions
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摘要 就固体酸催化剂对羧酸和酯类化合物的活化作用、相关的Friedel-Crafts反应催化体系和反应机理方面的研究进展进行了综述。其中,羧酸类化合物主要涉及饱和脂肪酸、芳基脂肪酸和烯酸;酯类化合物主要涉及直链酯和环状酯,重点是γ-丁内酯和丙二酸环亚异丙酯及其衍生物。特别是以烯酸、内酯或丙二酸环亚异丙酯为反应物,通过一步Friedel-Crafts反应可得到茚酮或萘酮类化合物,具有较高的应用价值,但是其工艺过程需要进一步的绿色化。开发新型催化剂及研究催化剂酸中心对反应物的活化机理是Friedel-Crafts反应绿色化的发展方向。 The research proceedings on application of carboxylic acids and esters in Friedel-Crafts reaction were reviewed, particularly for the activations of carboxylic acids and esters over solid acid catalysts, the effective catalyst system and the reaction mechanism. The carboxylic acids can be saturated, unsaturated or aromatic substituted alkanoic acid. The esters are straight-chain or cyclic ones, the latter mainly refer to y-butyrolactone, Meldrum' s acid and their derivatives. Especially, the compounds of indanone or tetralone can be obtained by using y-butyrolactone, unsaturated carboxylic acid and Meldrum' s acid as reactants in one-step by Friedel-Crafts reaction. These processes have high application value, but require further green. The further research to make Friedel-Crafls reactions green should be focused on developing new catalysts and studying the activation mechanism of reactants on the catalytic acid sites.
出处 《石油化工》 CAS CSCD 北大核心 2010年第3期233-240,共8页 Petrochemical Technology
基金 国家自然科学基金项目(20573094)
关键词 羧酸 内酯 茚酮 萘酮 Friedel—Crafts反应 固体酸催化剂 carboxylic acid ester lactone indanone tetralone Friedel-Crafts reaction solid acid catalyst
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  • 1OLSON C E, BADER A R. a-Tetralone E1 (2H)- Naphthalenone, 3,4-dihydro-3 [J]. Org Synth, 1963,4 : 898-898.
  • 2TRUCE W, OLSON C E. The aluminum chloride-cat alyzed condensation of r-butyrolactone with benzene [J]. J Am Chem Soc,1952,74(18):4721-4721.
  • 3BURZYNSKI S R, MUSIAL L. Synthesis of 4-pheny- lbutyric acid []. US:6,372,938B1,2002.
  • 4BANERJEE A K, VERA W, LAYA M S. A new synthesis of 5,8-dimethyl-2 tetralone-A potential inter- mediate for the synthesis of ring-A aromatic sesquiter- penes. Novel transformation during acetoxylation of 5, 8-dimethyldihydronapthalene( + ) [J]. Synth Comm, 2004,34 (12) : 2301-2308.
  • 5BATT D G, MAYNARD G D, PETRAITIS J J, et al. 2-Substituted-l-naphthols as potent 5-1ipoxygenase inhibitors with topical antiin{lammatory activity[J]. J Med Chem, 1990,33 ( 1 ) : 360-370.
  • 6BUETTELMANN B, ALANINE A, BOURSON A, et al. 2-Styryl-pyridines and 2-(3,4-Dihydro-naphtha- len-2-yl) pyridines as potent NR1/2B subtype selective NMDA receptor antagonists[J]. Chimia, 2004,58 (9) : 630-633.
  • 7KATRITZKY A R, MARSON C M, THIND S S, et al. The synthesis of some highly strained pyrylium and N-benzylpyridinium salts and kinetics of their reactions with piperidine[J]. J Chem Soe Perkin Trans I, 1983, 3:487-496.
  • 8JUNG K Y, KOREEDA M. Synthesis of 1,4-Dimeth- ylphenanthrenes, 2,4-Dimethylphenanthrenes, And 3, 4-Dimethylphenanthrene-A novel deoxygenation of are- ne 1,4-Endoxides with trimethylsilyl iodide[J]:I Org Chem, 1989,54(24) :5667-5675.
  • 9MAO J X, NAKAJO T, OKUHARA T. Alkylation- acylation of aromatics with gamma-butyrolactone cat- alyzed by heteropolyacids supported on silica [J].Chem Lett,2002,11 : 1104-1105.
  • 10KAMIYA Y, OOKA Y, OBARA C, et al. Alkyla- tion-acylation of p-xylene with )'-butyrolactone or vi- nylacetic acid catalyzed by heteropolyaeid supported onsilica[J]. J Mol Catal A: Chem,2007,262(1,2): 77-85.

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