Generic placeholder image

Current Green Chemistry

Editor-in-Chief

ISSN (Print): 2213-3461
ISSN (Online): 2213-347X

Research Article

A Solvent-free Method for Synthesis of Dihydroangelicins using Microwaves

Author(s): Diego M. Ruiz, Juan C. Autino and Gustavo P. Romanelli*

Volume 3 , Issue 3 , 2016

Page: [242 - 247] Pages: 6

DOI: 10.2174/2213346104666170224101037

Price: $65

Abstract

Background: Dihydrofurocoumarins are a large family of compounds, among them, dihydroangelicins and dihydropsoralens, are present in various plant species with varied biological activity. Several strategies have been developed for synthesizing these compounds and various catalysts have been used for this purpose.

Methods: In this work, we report the synthesis of 8,9-dihydrofuran [2, 3-h] coumarins using allyloxycoumarin cycloaddition in sustainable conditions: absence of solvents, application of microwave radiation, and insoluble acid catalysis by means of heteropolyacids with Preyssler structure, [H14(NaP5MoW29O110)].

Conclusion: With these conditions, and testing sustainability by means of Eco-Scale and E-factor, we replace the use of solvents and mineral acids having a great impact on the environment with a solid, easily recoverable heteropolyacid.

Keywords: Dihydroangelicins, dihydrofurocoumarins, microwave radiation, green chemistry, heteropolyacid, Preyssler structure.

Graphical Abstract

Rights & Permissions Print Export Cite as
© 2022 Bentham Science Publishers | Privacy Policy