Issue 53, 2022

Acidic tributyl phosphonium-based ionic liquid: an efficient catalyst for preparation of diverse pyridine systems via a cooperative vinylogous anomeric-based oxidation

Abstract

In this study, an acidic phosphonium-based ionic liquid, namely tributyl(3-sulfopropyl)phosphonium trifluoroacetate, was designed and synthesized via a facile and green route. From an accurate perspective, the structure of the prepared ionic liquid was investigated using FT-IR, 1H NMR and 13C NMR spectroscopies, and EDX, elemental mapping and TGA/DTG analysis. In this intensive research, catalytic application of tributyl(3-sulfopropyl)phosphonium trifluoroacetate was explored for the preparation of diverse pyridine systems such as triaryl pyridines, 2-amino-3-cyanopyridines and indolyl pyridines via a cooperative vinylogous anomeric-based oxidation (CVABO). The observed results proved that prepared acidic phosphonium-based ionic liquid is a effective catalyst for the multicomponent synthesis of pyridines.

Graphical abstract: Acidic tributyl phosphonium-based ionic liquid: an efficient catalyst for preparation of diverse pyridine systems via a cooperative vinylogous anomeric-based oxidation

Supplementary files

Article information

Article type
Paper
Submitted
25 Jul 2022
Accepted
17 Nov 2022
First published
06 Dec 2022
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2022,12, 34730-34739

Acidic tributyl phosphonium-based ionic liquid: an efficient catalyst for preparation of diverse pyridine systems via a cooperative vinylogous anomeric-based oxidation

S. Jalali-Mola, M. Torabi, M. Yarie and M. A. Zolfigol, RSC Adv., 2022, 12, 34730 DOI: 10.1039/D2RA04631H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements