Acid‐Functionalised Magnetic Ionic Liquid [AcMIm]FeCl4 as Catalyst for Oxidative Hydroxylation of Arylboronic Acids and Regioselective Friedel–Crafts Acylation1. Issue 8 (17th July 2017)

• Record Type: Journal Article
• Authors: Saha, Arijit; Payra, Soumen; Dutta, Dipa; Banerjee, Subhash
• Is Part Of: ChemPlusChem. Volume 82:Issue 8(2017)
• Page Start: 1129
• Page End: 1134
• Publication Date: 2017-07-17
• Subjects: acylation -- homogeneous catalysis -- ionic liquids -- magnetic properties -- synthesis design; Chemistry -- Periodicals; 540.5
• DOI: 10.1002/cplu.201700221
• Languages: English
• ISSNs: 2192-6506

Abstract

Abstract: An acid‐functionalised, magnetic, room‐temperature ionic liquid, 1‐acyl‐3‐methylimidazolium tetrachloroferrate ([AcMIm]FeCl4 ), was synthesised and its optical, magnetic, and thermal properties were investigated. The magnetic moment (0.05402 emu in 2 T magnetic fields) showed strong paramagnetic behaviour, and thermogravimetric analysis indicated very good thermal stability with a decomposition temperature higher than 230 °C. Additionally, [AcMIm]FeCl4 efficiently catalysed the oxidative ipso ‐hydroxylation of arylboronic acids and regioselective Friedel–Crafts acylation without external organic solvent or additives, such as acids, base, and ligands. This functionalised ionic liquid, [AcMIm]FeCl4, was recycled and reused at least six times without significant loss of its catalytic properties and stability. Abstract : Attractive separation : The facile oxidative hydroxylation of arylboronic acids and regioselective Friedel–Crafts (F–C; see scheme) acylation of phenols is demonstrated by using an acid‐functionalized magnetic ionic liquid (MAIL), 1‐acyl‐3‐methylimidazolium tetrachloroferrate ([AcMIm]FeCl4 ), as a catalyst and reaction medium.