Friedel-Crafts acylation catalysed by heteropoly acids

被引:147
作者
Kaur, J
Griffin, K
Harrison, B
Kozhevnikov, IV [1 ]
机构
[1] Univ Liverpool, Dept Chem, Leverhulme Ctr Innovat Catalysis, Liverpool L69 7ZD, Merseyside, England
[2] Johnson Matthey, Royston SG8 5HE, Herts, England
关键词
heterogeneous catalysis; Freidel-Crafts reaction; acylation; heteropoly acid;
D O I
10.1006/jcat.2002.3592
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The Friedel-Crafts acylation of anisole (AN) with acetic anhydride (AA) in liquid phase catalysed by bulk and silica-supported heteropoly acids (HPA), mainly H3PW12O40 (PW), has been studied. The PW exhibit very high activity, yielding up to 98% para and 2-4% ortho isomer of methoxyacetophenone (MOAP) at 90-110degreesC and an AN/AA molar ratio of 10-20. Catalyst pretreatment is essential; the activity passes a maximum at a pretreatment temperature of 150degreesC. The acylation of anisole appears to be heterogeneously catalysed; no contribution of homogeneous catalysis by HPA was observed. PW is almost a factor of 100 more active than the zeolite H-beta, which is in agreement with the higher acid strength of HPA. The PW catalyst is reusable, although gradual decline of activity was observed due to the coking of the catalyst. The acylation is inhibited by product because of adsorption of MOAP on the catalyst surface. The ratio of adsorption coefficients of MOAP and anisole has been found to be 37 at 90degreesC. Anisole acylation is first order in acetic anhydride, the order in catalyst is 0.66, and the apparent activation energy is 41 kJ/mol in the temperature range of 70-110degreesC. In contrast to anisole, the acylation of toluene with HPA is far less efficient than that with H-beta. Evidence is provided that the activity of HPA in toluene acylation is inhibited by preferential adsorption of acetic anhydride on the catalyst. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:448 / 455
页数:8
相关论文
共 20 条
  • [1] [Anonymous], J MOL CATAL A
  • [2] ELECTROPHILIC AROMATIC SUBSTITUTION REACTIONS
    BERLINER, E
    [J]. PROGRESS IN PHYSICAL ORGANIC CHEMISTRY, 1964, 2 : 253 - 321
  • [3] FRIEDEL-CRAFTS ACYLATION OF TOLUENE AND PARA-XYLENE WITH CARBOXYLIC-ACIDS CATALYZED BY ZEOLITES
    CHICHE, B
    FINIELS, A
    GAUTHIER, C
    GENESTE, P
    GRAILLE, J
    PIOCH, D
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (11) : 2128 - 2130
  • [4] DESIGN OF SYNTHETIC ZEOLITES AS CATALYSTS IN ORGANIC-REACTIONS - ACYLATION OF ANISOLE BY ACYL CHLORIDES OR CARBOXYLIC-ACIDS OVER ACID ZEOLITES
    CORMA, A
    CLIMENT, MJ
    GARCIA, H
    PRIMO, J
    [J]. APPLIED CATALYSIS, 1989, 49 (01): : 109 - 123
  • [5] Zeolite catalysts as solid solvents in fine chemicals synthesis - 2. Competitive adsorption of the reactants and products in the Friedel-Crafts acetylations of anisole and toluene
    Derouane, EG
    Crehan, G
    Dillon, CJ
    Bethell, D
    He, H
    Derouane-Abd Hamid, SB
    [J]. JOURNAL OF CATALYSIS, 2000, 194 (02) : 410 - 423
  • [6] Zeolite catalysts as solid solvents in fine chemicals synthesis - 1. Catalyst deactivation in the Friedel-Crafts acetylation of anisole
    Derouane, EG
    Dillon, CJ
    Bethell, D
    Derouane-Abd Hamid, SB
    [J]. JOURNAL OF CATALYSIS, 1999, 187 (01) : 209 - 218
  • [7] Silica-included heteropoly compounds as solid acid catalysts
    Izumi, Y
    Ono, M
    Kitagawa, M
    Yoshida, M
    Urabe, K
    [J]. MICROPOROUS MATERIALS, 1995, 5 (04): : 255 - 262
  • [8] Izumi Y., 1992, Zeolite, Clay and Heteropoly Acid in Organic Reactions
  • [9] Catalysis by heteropoly acids and multicomponent polyoxometalates in liquid-phase reactions
    Kozhevnikov, IV
    [J]. CHEMICAL REVIEWS, 1998, 98 (01) : 171 - 198
  • [10] Coking and regeneration of H3PW12O40/SiO2 catalysts
    Kozhevnikov, IV
    Holmes, S
    Siddiqui, MRH
    [J]. APPLIED CATALYSIS A-GENERAL, 2001, 214 (01) : 47 - 58