Synthesis of quinazolines over recyclable Fe3O4@SiO2-PrNH2-Fe3+ nanoparticles: A green, efficient, and solvent-free protocol

  • Esmaiel Eidi
  • , Mohamad Z. Kassaee*
  • , Zahra Nasresfahani
  • , Peter T. Cummings
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

A practical and efficient method is developed for efficient synthesis of quinazoline derivatives through condensation reaction of 2-aminoaryl ketone, an aldehyde, and ammonium acetate, over magnetic Fe3O4@SiO2-PrNH2-Fe3+ NPs as a recyclable nanocatalyst, under solvent-free conditions. The as-prepared nanocatalyst was characterized using Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), and vibrating sample magnetometer (VSM). Mild conditions, easy work up, high purity of the products, recyclability, readily availability, nontoxicity, economical, and environmental-friendly nature of the iron catalyst are the attractive features of this methodology.
Original languageEnglish
Article numbere4573
JournalApplied Organometallic Chemistry
Volume32
Issue number12
DOIs
Publication statusPublished - Dec 2018

Keywords

  • Iron catalyst
  • Magnetic nanoparticles
  • Quinazoline
  • Recyclable
  • Solvent-free

ASJC Scopus subject areas

  • General Chemistry
  • Inorganic Chemistry

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