Scinovex
article

Friedel-Crafts alkylation and acylation of aromatic compounds under solvent free conditions using solid acid catalysts

International Journal of Chemical Studies · 2015 · Vol. 2(5) · pp. 27–34

Abstract

Solid acid catalysts, M(IV) Phosphotungstates [M(IV)PWs], mixed materials of the class of TMBA (Tetravalent Metal Bianionic Acid) salts and 12-Tungstophosphoric acid (12-TPA) supported onto M(IV) Oxides [M(IV) = Zr, Ti, Sn] have been synthesized and their utility towards Friedel–Crafts alkylation and acylation reactions has been explored and compared. The catalysts have been characterized for elemental analysis by ICP-AES, TGA, FTIR, SEM, EDX, XRD, surface area (BET) and surface acidity (NH3TPD). Friedel-Crafts alkylation and acylation have been studied as model reactions under solvent free conditions wherein acetyl chloride is used for acylation of anisole/veratrole and benzyl chloride is used for alkylation of toluene. Reaction conditions have been optimized by varying parameters such as reaction time, reaction temperature, catalyst amount and mole ratio of the reagents. Highlighting features are selectivity of products under solvent free conditions and regeneration/reuse of catalysts without much loss in % yields.

Polyoxometalates: Synthesis and ApplicationsChemical Synthesis and ReactionsChemical Synthesis and CharacterizationFriedel–Crafts reactionAlkylationAcylationChemistryBenzyl chlorideCatalysisBenzoyl chlorideAnisoleSolventToluene
Citations
4
FWCI
0.28
field-weighted impact
References
21
Percentile
57%
vs. same field & year
Citations per year
References
Sulfated zirconia and its modified versions as promising catalysts for industrial processes
Microporous and Mesoporous Materials · 1999 · 704 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.