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Regioselectivity of Friedel-Crafts acylation of aromatic compounds with several cyclic anhydrides

✍ Scribed by Iwao Hashimoto; Takatoshi Kawaji; Florin D. Badea; Tsuyoshi Sawada; Shuntaro Mataka; Masashi Tashiro; Gouki Fukata


Book ID
114996547
Publisher
Springer Netherlands
Year
1996
Tongue
English
Weight
622 KB
Volume
22
Category
Article
ISSN
0922-6168

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Friedel-Crafts acylation is carried out with several aromatic substrates in the presence of an electrochemically active aluminium anode to minimize the inorganic reagents. Only a catalytic amount of AlCl 3 (5 mol %) is required to enable the anodic polarization of the aluminium electrode to promote

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The stable and non-hygroscopic aluminum dodecatungstophosphate (AlPW 12 O 40 ), was found to be an effective catalyst (3 mol%) for the solvent-free Friedel-Crafts acylation of aromatic compounds with carboxylic acids in the presence of trifluoroacetic anhydride under mild reaction conditions.