Solid-supported Friedel-Crafts acylation

Type of reaction C-C bond formation Reaction conditions Solvent-free, room temperature Synthetic strategy Solid-supported Friedel-Crafts acylation Catalyst Zinc oxide (ZnO) powder... 

The ability of iron(III) chloride genuinely to catalyze Friedel-Crafts acylation reactions has also been recognized by Holderich and co-workers [97]. By immobilizing the ionic liquid [BMIM]Cl/FeCl3 on a solid support, Holderich was able to acetylate mesitylene, anisole, and m-xylene with acetyl chloride in excellent yield. The performance of the iron-based ionic liquid was then compared with that of the corresponding chlorostannate(II) and chloroaluminate(III) ionic liquids. The results are given in Scheme 5.1-67 and Table 5.1-5. As can be seen, the iron catalyst gave superior results to the aluminium- or tin-based catalysts. The reactions were also carried out in the gas phase at between 200 and 300 °C. The acetylation reac-... 

The first example of SILP-catalysis was the fixation of an acidic chloroaluminate ionic liquid on an inorganic support. The acidic anions of the ionic liquid, [AI2CI7] and [AI3CI10], react with free OH-groups of the surface to create an anionic solid surface with the ionic liquid cations attached [72]. The catalyst obtained was applied in the Friedel-Crafts acylation of aromatic compounds. Later, the immobilisation of acidic ionic liquids by covalent bonding of the ionic liquid cation to the surface was developed and applied again in Friedel-Crafts chemistry [73]. 

In-situ IR-spectroscopic characterization of the Friedel-Crafts acylation of benzene in ionic liquids derived from AICI3 and FeCl3 showed that the mechanism of the reaction in ionic liquids was the same as that in 1,2-dichloroethane (128). The immobilization of ferric chloride-containing ionic liquid onto solid supports (e.g., silica and carbon) however failed to catalyze the acylation reaction, because leaching was a serious problem. When the reaction was carried out with gas-phase reactants, catalyst deactivation was observed. 

Maximum effort has been directed toward the use of solid acid catalysts. In fact, heterogeneous catalysts can be easily separated from the reaction mixture and reused they are generally not corrosive and do not produce problematic side products. Different classes of materials have been studied and utilized as heterogeneous catalysts for Friedel-Crafts acylations these include zeolites (acid treated), metal oxides, and heteropoly acids already utilized in hydrocarbon reactions. Moreover, the application of clays, perfluorinated resinsulfonic acids, and supported (fluoro) sulfonic acids, mainly exploited in the production of fine chemicals, are the subject of intensive studies in this area. 

The use of HPAs and multicomponenf polyoxometalates as catalysts in liquid-phase reactions was reviewed by Kozhevnikov. Moreover, an interesting minireview was published concerning the Friedel-Crafts acylation of arenes and the Fries rearrangement catalyzed by HPA-based solid acids. The results show that HPA-based solid acids, including bulk and supported heteropoly acids as well as heteropoly acid salts, are efficient and environmentally friendly catalysis for all reacfions analyzed. 

Hu, R.-J. and Li, B.-G. 2004. Novel solid acid catalyst, bentonite-supported polytrifluoromethanesulfosiloxane for Friedel-Crafts acylation of ferrocene. Catal. Lett. 98 43 7. 

Work on similar supported Lewis-acidic catalysts was further extended to a variety of Friedel-Crafts alkylation [7] and acylation [8] reactions (see Section 5.2.2.4). In these investigations the catalysts are simply prepared by the addition of a liquid to a solid support. A typical catalyst preparation [9] involves treating a previously dried... 

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