Journal
MOLECULES
Volume 28, Issue 18, Pages -Publisher
MDPI
DOI: 10.3390/molecules28186747
Keywords
ionin liquid; polymer supported ionic liquid; nucleophilic fluorination; heterogeneous promoter
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In this study, hexaethylene glycolic vinyl imidazolium was supported on N-vinyl caprolactam to form a heterogeneous catalyst for aliphatic nucleophilic substitution reactions using alkali metal salts. The catalyst showed high activity, selectivity, and stability, resulting in higher yields and reduced formation of by-products. This study demonstrates the efficiency of nucleophilic fluorination and substitution reactions in various sulfonyloxyalkanes and haloalkanes.
Hexaethylene glycolic vinyl imidazolium (hexaEGVIM) was supported on N-vinyl caprolactam via covalent bonds through simple copolymerization to form poly caprolactam-supported hexaethylene glycol-substituted imidazolium salts (PCLS-hexaEGIM). The resulting heterogeneous PCLS-hexaEGIM promoter was active, selective, and stable for aliphatic nucleophilic substitution reactions using alkali metal salts. The alkali metal salts dramatically enhanced the reactivity of this heterogeneous catalyst with easily isolable higher product yields, reducing the formation of by-products. Therefore, nucleophilic fluorination and other substitution reactions can act as highly efficient catalysts in various sulfonyloxyalkanes and haloalkanes with regard to their corresponding fluorinated products.
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