Article ID Journal Published Year Pages File Type
65150 Journal of Molecular Catalysis A: Chemical 2014 9 Pages PDF
Abstract

•Epoxide phenolysis.•Neutral condition.•Silver nanoparticles.•Recyclable catalyst.•Drug synthesis.

Chemo- and regio-selective epoxide phenolysis is reported for the first time under neutral condition catalysed by silver nanoparticles. Other metal nanoparticles (e.g., Au, Pd, Cu, In, and Ru) are less effective. The choice of solvent is critical with 2-propanol being the best followed by DEF. Amongst various stabilisers used (surfactants, PEGs, tetra-alkylammonium halides) the tetra-alkylammonium halides are found to be the most effective (TBAF > TBAB > TBACl > TBAI). The role of the silver nanoparticles is envisaged as synchronous mode epoxide-phenol dual activation via a cooperative network of coordination, anion–π interaction, and hydrogen bond. The silver nanoparticles are recovered and reused for five consecutive times. The reaction has been used for the synthesis of propranolol and naftopidil as a few representative cardiovascular drugs.

Graphical abstractSynergistic activation of epoxide-phenol dual activation catalysed by in situ generated silver nanoparticles is reported for the first time for epoxide phenolysis under base-free conditions that finds application towards the synthesis of various drug molecules.Figure optionsDownload full-size imageDownload high-quality image (74 K)Download as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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