# Piperazine-grafted magnetic graphene oxide as a sustainable heterogeneous catalyst for solvent-free Biginelli reaction

**Authors:** Esmail Rezaei-Seresht, Faezeh Jalambadani, Samira Cheshak, Behnam Mahdavi, Fatemeh Tafazzoli Gazkoh

PMC · DOI: 10.1039/d5ra05063d · RSC Advances · 2026-02-24

## TL;DR

Researchers created a reusable magnetic catalyst for a key chemical reaction, making it more eco-friendly and cost-effective.

## Contribution

A novel heterogeneous Fe3O4@GO-NH catalyst was developed for the solvent-free Biginelli reaction.

## Key findings

- The Fe3O4@GO-NH nanocomposite showed high catalytic activity under solvent-free conditions.
- 32 Biginelli products were synthesized with high yields using the new catalyst.
- The catalyst is reusable, offering environmental and cost benefits over traditional methods.

## Abstract

Multi-component reactions (MCRs) are powerful tools for the one-pot synthesis of complex organic compounds, with the Biginelli reaction being one of the most important due to its versatility in synthesizing a wide range of dihydropyrimidine-2-ones (DHPMs) with diverse biological activities. However, traditional MCR catalysts are often homogeneous and challenging to recycle, leading to environmental concerns and high costs. In this study, we developed a novel heterogeneous catalyst for the Biginelli reaction by functionalizing graphene oxide (GO) with piperazine (NH) to form a Fe3O4@GO-NH nanocomposite. The catalyst was characterized using FT-IR, TGA, and SEM/EDX and showed high catalytic activity for the Biginelli reaction under solvent-free conditions. The optimal reaction conditions were determined by adjusting various parameters such as temperature, stability and reproducibility, time, and the molar percentage of Fe3O4@GO-NH. As a result of this eco-friendly approach, 32 Biginelli products were successfully obtained with high yields. The catalyst was also reusable, making it a more environmentally friendly and cost-effective alternative to conventional homogeneous catalysts.

Biginelli reaction is a powerful tool for the one-pot synthesis of complex organic compounds, due to its versatility in synthesizing a wide range of dihydropyrimidine-2-ones (DHPMs) with diverse biological activities.

## Full-text entities

- **Genes:** NR3C2 (nuclear receptor subfamily 3 group C member 2) [NCBI Gene 4306] {aka MCR, MLR, MR, NR3C2VIT}
- **Diseases:** weight loss (MESH:D015431), inflammatory (MESH:D007249), neurodegenerative, cardiovascular, and metabolic disorders (MESH:D019636), tumor (MESH:D009369)
- **Chemicals:** ethyl acetate (MESH:C007650), graphite (MESH:D006108), Ethyl 4-(4-chlorophenyl)-6-methyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate (-), 2H (MESH:D003903), proton (MESH:D011522), urea (MESH:D014508), toluene (MESH:D014050), acetone (MESH:D000096), Piperazine (MESH:D000077489), epoxide (MESH:D004852), H (MESH:D006859), KCl (MESH:D011189), ice (MESH:D007053), methanol (MESH:D000432), silica gel (MESH:D058428), ethyl acetoacetate (MESH:C024840), metal (MESH:D008670), ammonia (MESH:D000641), oxygen (MESH:D010100), n-hexane (MESH:C026385), acids (MESH:D000143), N (MESH:D009584), benzaldehyde (MESH:C032175), GO (MESH:C000628730), CO (MESH:D002248), C (MESH:D002244), water (MESH:D014867), Fe (MESH:D007501), acetic acid (MESH:D019342), C-Cl (MESH:D002433), Cu (MESH:D003300), KBr (MESH:C039004), thiourea (MESH:D013890), Aldehyde (MESH:D000447), dihydropyridine (MESH:C038806), ethanol (MESH:D000431)

## Full text

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## Figures

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## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12930250/full.md

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Source: https://tomesphere.com/paper/PMC12930250