Phthalimide-N-sulfonic acid and Isatin-N-sulfonic acid as highly efficient catalysts for the synthesis of bis-coumarins
Journal: Iranian Chemical Communication (Vol.6, No. 4)Publication Date: 2018-10-01
Authors : Abdolkarim Zare; Jalal Sanjideh;
Page : 416-422
Keywords : 4-hydroxycoumarin; arylaldehyde; bis-coumarin; phthalimide-N-sulfonic acid (PhtSA); isatin-N-sulfonic (IsSA); SO3H-bearing solid acid;
Abstract
Two highly efficient protocols for the production of bis-coumarins under solvent-free conditions have been introduced. The reaction of 4-hydroxycoumarin (2 eq.) with arylaldehydes (1 eq.) using phthalimide-N-sulfonic acid (PhtSA) or isatin-N-sulfonic acid (IsSA), as solid-acid catalysts, afforded the mentioned compounds with good to excellent yields in short times.Briefly, we have introduced two new SO3H-bearing solid-acid catalysts, entitled phthalimide-N-sulfonic acid and isatin-N-sulfonic acid, for the preparation of bis-coumarins. The advantages of the presented protocols include: high effectuality and generality of the catalysts, high to excellent yields, short reaction times, simple synthesis of the catalysts from available and inexpensive starting materials, easy work-up and purification of the products, relatively mild conditions, application of solvent-free technique, and good compliance with the green chemistry protocols.
Other Latest Articles
- Green and efficient synthesis of propargylamines via A3 coupling reaction using a copper (II)–thioamide combination
- Application of nano TiO2@KSF as an efficient and reusable catalyst for the synthesis of pyrano-pyrimidines
- A mild protocol for the preparation of 2-amino-dihydropyrano[3,2-b] pyran-3-carbonitriles via cobalt nanoparticles-catalyzed multi-component reaction in water
- Electrocatalytic multicomponent assembling of aldehydes, dimedone and 1-naphthylamine for synthesis of novel tetrahydrobenzo[c]acridin-8(7H)-one derivatives
- Preparation and evaluation of some newly liquid crystal as antioxidant for base stocks
Last modified: 2019-06-26 14:27:01