Application of Fe <sub>3</sub> O <sub>4</sub> @SiO <sub>2</sub> @APIDSO <sub>3</sub> H as a Novel Magnetic Nanocatalyst in Domino‐Knoevenagel–Phospha‐Michael Reaction

Abstract This research describes a synthesis method using Fe 3 O 4 @SiO 2 @APIDSO 3 H as a magnetic nanocatalyst for preparing α‐substituted phosphonates by domino‐Knoevenagel–phospha‐Michael reaction. The reaction involves 1,3‐dicarbonyl compounds (dimedone and 1,3‐dimethyl barbituric acid) reacting with different aromatic aldehydes and triethyl phosphite. The Fe 3 O 4 @SiO 2 @APIDSO 3 H catalyst was previously prepared and characterized. The synthesized products were identified using 1 H‐NMR, 13 C‐NMR, 31 P‐NMR, FT‐IR spectroscopy, and CHNS analysis. The resulting compounds possess reactive functional groups in their structure, making them suitable as building blocks for further chemical modifications in medicinal and biochemical applications. This approach also offers advantages like catalyst recovery and reusability, short reaction times, and simplified workup procedures.

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Publication Details

Journal
ChemistrySelect
Published
2025-09-25
DOI
https://doi.org/10.1002/slct.202501853
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
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article

Application of Fe 3 O 4 @SiO 2 @APIDSO 3 H as a Novel Magnetic Nanocatalyst in Domino‐Knoevenagel–Phospha‐Michael Reaction

Soheila Ghassamipour, Arezu Jamalian, Masoomeh Emadi, Zohre Aghashiri
ChemistrySelect
Multicomponent Synthesis of Heterocycles
article

Application of Fe 3 O 4 @SiO 2 @APIDSO 3 H as a Novel Magnetic Nanocatalyst in Domino‐Knoevenagel–Phospha‐Michael Reaction

Soheila Ghassamipour, Arezu Jamalian, Masoomeh Emadi, Zohre Aghashiri
article en

Abstract

Abstract This research describes a synthesis method using Fe 3 O 4 @SiO 2 @APIDSO 3 H as a magnetic nanocatalyst for preparing α‐substituted phosphonates by domino‐Knoevenagel–phospha‐Michael reaction. The reaction involves 1,3‐dicarbonyl compounds (dimedone and 1,3‐dimethyl barbituric acid) reacting with different aromatic aldehydes and triethyl phosphite. The Fe 3 O 4 @SiO 2 @APIDSO 3 H catalyst was previously prepared and characterized. The synthesized products were identified using 1 H‐NMR, 13 C‐NMR, 31 P‐NMR, FT‐IR spectroscopy, and CHNS analysis. The resulting compounds possess reactive functional groups in their structure, making them suitable as building blocks for further chemical modifications in medicinal and biochemical applications. This approach also offers advantages like catalyst recovery and reusability, short reaction times, and simplified workup procedures.

ChemistrySelectVol. 10(37)
Islamic Azad University, Marvdasht (IR)
Openalex Percentile: Top 80%
Multicomponent Synthesis of Heterocycles
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