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Thiocyanation and 2-Amino-1,3-thiazole Formation in Water Using Recoverable and Reusable Glycosylated Resorcin[4]arene Cavitands

Ali Husain, Kirpal S. Bisht

2020The Journal of Organic Chemistry20 citationsDOI

Abstract

A family of three spatially directional resorcin[4]arene cavitand glycoconjugates (RCGs) have been applied as efficient recoverable and reusable inverse phase transfer catalysts for eco- and environmentally friendly thiocyanation and 2-amino-1,3-thiazole formation reactions in water. The results show that RCGs (1 mol %) were capable of hosting and catalyzing various water-insoluble bromo/thiocyanato substrates in water without the use of any co-organic solvents. The recoverability and reusability of RCG catalytic systems, that is, RCG1 and RCG3, were also examined upon a simple extraction of the desired products using DCM or ethyl acetate, followed by subjecting the recovered aqueous solution containing the RCG catalysts to the next reaction cycles.

Topics & Concepts

ChemistryCavitandCatalysisThiazoleEnvironmentally friendlyExtraction (chemistry)ReusabilityAqueous solutionCombinatorial chemistryOrganic chemistrySolid phase extractionSupramolecular chemistryMoleculeComputer scienceEcologySoftwareBiologyProgramming languageSynthesis and Characterization of Heterocyclic CompoundsChemical Synthesis and AnalysisChemical Synthesis and Reactions
Thiocyanation and 2-Amino-1,3-thiazole Formation in Water Using Recoverable and Reusable Glycosylated Resorcin[4]arene Cavitands | Litcius