| Authors | ستاره موسوی,حسین نعیمی,امیرحسین قاسمی,شادان کرمانی زاده |
| Journal | Scientific Reports |
| Page number | 10840 |
| Volume number | 13 |
| IF | 4.6 |
| Paper Type | Full Paper |
| Published At | 2023-07-05 |
| Journal Grade | Scientific - research |
| Journal Type | Electronic |
| Journal Country | Iran, Islamic Republic Of |
| Journal Index | SCOPUS ,JCR |
Abstract
Pyrroles are widely spread worldwide because of their critical applications, especially pharmacology.
An expedition method for one-pot synthesis of N-substituted pyrrole derivatives has been presented
by a reaction between 2,5-dimethoxytetrahydrofuran and various primary aromatic amines in the
presence of NiFe2O4
anchored to modified carbon hollow microspheres (
NiFe2O4@MCHMs) as a
recoverable reactive catalyst. The Classon-Kass method has been used to synthesize the pyrroles
in excellent yields and short reaction times in the same direction with green chemistry rules. This
reaction was carried out by employing NiFe2O4@
MCHMs as a catalyst to make a simple procedure
with short activation energy in water as an accessible, non-toxic, and biodegradable solvent. This
catalyst provides a promising pathway to synthesize N-substituted pyrroles several times in a row
through the recyclability without remarkable loss of its catalytic activity. The NiFe2O4@
MCHMs
nanocatalyst was characterized by applying FT-IR, XRD, FE-SEM, TEM, EDS, BET, TGA, VSM, and
elemental mapping techniques. Also, the synthesized N-substituted pyrrole derivatives were
identified using melting point, FT-IR, and 1H NMR analyses.