*Corresponding author:
Farahnaz K Behbahani, Department of Chemistry, Karaj Branch, Islamic Azad University, P.O. Box 314/85313 Karaj, IranReceived: January 03, 2018; Published: January 09, 2018
DOI: 10.26717/BJSTR.2018.02.000655
To view the Full Article Peer-reviewed Article PDF
A fast, efficient and versatile route for the synthesis of 4,4’-diaminotriarylmethanes using Sr(DS)2 as a Lewis acid-surfactant-combined catalyst, LASCs in the presence of N,N-dimethyl aniline and aryl aldehydes is reported. LASCs not only act as a Lewis acid to activate substrate molecules, but also serve as a surfactant to form stable colloidal dispersion systems with organic substrates. Also, the others advantages of LASCs are easy separation and recovery, high activity, selectivity, as a Lewis acid to activate the substrate molecules and as a surfactant to help to solubilize the organic compounds in water. In this project a variety of aryl aldehydes were subjected to synthesize of 4,4’-diaminotriarylmethanes in the presence of strontiumdodeceyl sulfate, N,N-dimethyl aniline under solvent free condition and at 100 °C%.
Keywords: Sr(DS)2; N,N-dimethyl aniline; Aldehyde; Catalyst; Surfactanty
Abstract| Introduction| Experimental Procedure| Results and Discussion| Conclusion| References|
International Association of Landscape Archaeology, Czech Glass Society, Czech Republic
Department of Chemistry, Semenov Institute of Chemical Physics, USSR Academy of Sciences, Moscow, Russia
Pharmaco-kinetics, dynamics and Drug Metabolism, Touro College of Pharmacy, USA
Professor of Nuclear Medicine, Faculty of Medicine and Surgery, University of Milan, Milan, Italy
Associate Professor at Department of Breast and Thyorid Surgey, Chongqing General Hospital, China