Synthesis, Characterization, and Application of a Novel Polystyrene-Supported Brønsted-Acidic Ionic Liquid as an
Nicolas S Anjos1, Daniel P Marques1, Sandy J Coutinho1
1Department of Pharmaceutical Sciences, Federal University of São PauloUNIFESP, Rua São Nicolau 210, Diadema, São Paulo 09913-030, Brazil.
Abstract:
Herein, we report a novel synthesis of the polymer-supported Brønsted-acidic ionic liquidPS-[(SO3H)4C4Im]-[OTf]as an efficient and recyclable heterogeneous catalyst for the Groebke-Blackburn-Bienaymé (GBB) multicomponent reaction. The catalyst was synthesized from Merrifield resin (polystyrene) and fully characterized by thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Its catalytic activity was then evaluated in GBB model reactions, with the optimal conditions determined using 50 mg mmol-1 of PS-[(SO3H)4C4Im]-[OTf] in ethanol as solvent under microwave heating at 150 °C for 1 h. A diverse library of imidazo-fused heterocycles (e.g., imidazo-[1,2-a]-pyridines, imidazo-[2,1-b]-thiazoles, and benzo-[d]-imidazo-[2,1-b]-thiazoles) was synthesized using the optimized conditions and the corresponding products were obtained in moderate to excellent yields (34-91%), depending on the starting aminoazole. Furthermore, the heterogeneous catalyst could be easily recovered by filtration after each reaction cycle and reused for up to six consecutive cycles with no significant loss of integrity as well as catalytic activity (average yield 86 ± 3.5%). These results demonstrated the potential of this polymer-supported Brønsted-acidic ionic liquid as a sustainable catalyst for acid-catalyzed multicomponent reactions applied to the synthesis of nitrogen-based heterocycles of interest in Medicinal Chemistry.
Related Concept Videos
Olefin Metathesis Polymerization: Overview
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction
Radical Anti-Markovnikov Addition to Alkenes: Overview
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
Radical Substitution: Allylic Bromination


