Issue 78, 2014

Synthesis of dibenzoxanthene and acridine derivatives catalyzed by 1,3-disulfonic acid imidazolium carboxylate ionic liquids

Abstract

New members of 1,3-disulfonic acid imidazolium carboxylate ionic liquids [DSIM][X] (where X = [CH3COO], [CCl3COO], [CF3COO]) were prepared and characterized by 1H NMR,13C NMR, FT-IR, TGA,UV-vis and elemental analysis. The more acidic ILs [DISM][CCl3COO] and [DSIM][CF3COO] were efficiently utilized as recyclable catalysts for the preparation of 14H-dibenzo[a,j]xanthene and 1,8-dioxo-decahydroacridine derivatives in short times under solvent-free conditions at 80–100 °C with excellent yields. The above two ILs could be effectively utilized as catalysts for the synthesis of 1,8-dioxo-decahydroacridine in water at the same temperature.

Graphical abstract: Synthesis of dibenzoxanthene and acridine derivatives catalyzed by 1,3-disulfonic acid imidazolium carboxylate ionic liquids

Supplementary files

Article information

Article type
Communication
Submitted
19 Jul 2014
Accepted
27 Aug 2014
First published
27 Aug 2014

RSC Adv., 2014,4, 41287-41291

Author version available

Synthesis of dibenzoxanthene and acridine derivatives catalyzed by 1,3-disulfonic acid imidazolium carboxylate ionic liquids

A. K. Dutta, P. Gogoi and R. Borah, RSC Adv., 2014, 4, 41287 DOI: 10.1039/C4RA07323A

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