Effects of acyl donor type, catalyst type, and reaction conditions on the activity and selectivity of Friedel-Crafts acylation

Wolfson, Adi, Madhusudhan, Rao P., Shapira-Tchelet, Ayelet and Landau, Miron V. Effects of acyl donor type, catalyst type, and reaction conditions on the activity and selectivity of Friedel-Crafts acylation Chemical Papers, Vol.63, No. 3, 2009, 291-297

Document type: Článok z časopisu / Journal Article
Collection: Chemical papers  

Author(s) Wolfson, Adi
Madhusudhan, Rao P.
Shapira-Tchelet, Ayelet
Landau, Miron V.
Title Effects of acyl donor type, catalyst type, and reaction conditions on the activity and selectivity of Friedel-Crafts acylation
Journal name Chemical Papers
Publication date 2009
Year available 2009
Volume number 63
Issue number 3
ISSN 0366-6352
Start page 291
End page 297
Place of publication Poland
Publisher Versita
Collection year 2009
Language english
Subject 250000 Chemical Sciences
Abstract/Summary Acylation of anisole and 3-methylanisole was performed with several acylating reagents (acetylation by AcCl and Ac2O and bromoacetylation by BrAcCl and (BrAc)2O) over different solid acid catalysts. The reaction conditions were optimized with respect to the acylation reagent, overall yield, solid acid catalyst, and the products selectivities. While acylation of anisole with acetyl chloride or acetic anhydride resulted in its full conversion to para-substituted acetophenone, the use of bromoacetyl bromide or bromoacetic anhydride yielded also the ortho-substituted product. Acylation of 3-methylanisole also yielded both para- and ortho-substitutions, and the products distribution was affected by the reaction conditions and catalyst type. It was found that while more acidic catalysts (caesium salt of heteropolyacid and zeolites) were the most active towards anisole acylation, the most active catalysts for the acylation of 3-methylanisole were ion-exchange catalysts. Employing HY-740 zeolite resulted in the highest ortho-selectivity in the acylation of anisole with bromoacetyl bromide and bromoacetic anhydride and in the acylation of 3-methylanisole with acetic anhydride.
 
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