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Paper ID:10.55041/IJSREM.ISTCESD052

Ag STA: Green and an Efficient Catalyst for Synthesis of Benzimidazole Derivatives at Room Temperature

Stream/Area:

-

Subject:

-

Paper ID:

10.55041/IJSREM.ISTCESD052

Volume:

10 |

9 |

Sep 2026

Pages:

1-5

Publication Frequency:

Monthly (12 issues per year)

DOI
Digital Object Identifier
10.55041/ijsrem.ISTCESD052

License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.

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Authors

MBS

Mantosh B. Swami

Chemistry

Mahatma Basweshwar College, Latur (Maharashtra)

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SRM

Sushil R. Mathapati

Chemistry

Mahatma Basweshwar College, Latur (Maharashtra)

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Abstract

A recyclable heterogeneous catalyst was prepared and successfully employed for the simple, convenient, and efficient one-pot synthesis of substituted benzimidazole derivatives from *o*-phenylenediamine and aryl aldehydes. The silver salt of silicotungstic acid was found to be an economical and reusable catalyst, affording the desired products with a low catalyst loading of 10 mol%. The reactions proceeded smoothly to give moderate to high yields (61–86%) within 4.5–10 h. The recyclability of the catalyst, together with its simple operation and efficient catalytic performance, demonstrates the potential of this protocol as a greener approach to the synthesis of substituted benzimidazole derivatives.

KEYWORDS

Ag STA efficient synthesis o-phenylene diamine benzimidazole room temperature.

Cite This Article

Mantosh B. Swami, Sushil R. Mathapati, "Ag STA: Green and an Efficient Catalyst for Synthesis of Benzimidazole Derivatives at Room Temperature," International Journal of Scientific Research in Engineering and Management, vol. 10, no. 9, pp. 1-5, Sep 2026. https://doi.org/10.55041/ijsrem.ISTCESD052

Full Article/Conclusion

In the present study, an efficient one-pot, solvent-free protocol has been developed for the synthesis of substituted benzimidazole derivatives at room temperature using silver silicotungstate (Ag-STA) as a recyclable heterogeneous catalyst. The catalyst was prepared according to a reported literature procedure and successfully applied to the cyclocondensation of *o*-phenylenediamines with aromatic aldehydes. Under the optimized conditions, the use of 10 mol% Ag-STA afforded complete conversion of the starting materials and the corresponding benzimidazole products in yields of up to 86%. The catalyst could be recovered and reused for up to six consecutive cycles without a significant loss in catalytic performance or product selectivity. The developed protocol offers several practical advantages, including simple operation, mild reaction conditions, solvent-free processing, straightforward work-up, and catalyst recyclability. These features make the Ag-STA-catalyzed methodology a useful approach for the synthesis of substituted benzimidazole derivatives.

References

[1] D. A. Horton, G. T. Bourne, and M. L. Sinyth. Chemical Reviews, 2003; 103:3, 893–930. [2] M. Alamgir, C. D. Black, and N. Top Kumar, Heterocyclic Chemistry, 2007; 9, 87–118 [3] A. R. Porcari, R. V. Devivar, L. S. Kucera, J. C. Drach, and L. B. Townsend, Journal of Medicinal Chemistry, 1998; 41, 8, 1252–1262. [4] T. Roth, M. L. Morningstar, P. L. Boyer, S. H. Hughes, R. W. Buckheit, and C. J. Michejda,  Journal of Medicinal Chemistry, 1997; 40: 26, 4199–4207. [5] M. T. Migawa, J. L. Girardet, J. A. Walker et al., Journal of Medicinal Chemistry, 1998; 41: 8,1242–1251. [6] I. Tamm and P. B. Sehgal, Advances in Virus Research, 1978; 22, 187–258. [7] I. Tamm, Science, 1954;120: 3125, 847–848. [8] Z. Kazimierczuk, M. Andrzejewska, J. Kaustova, and V. Klimesova, European Journal of Medicinal Chemistry, 2005; 40: 2, 203–208. [9] Oren I Y, Yalcin I, Sener E A, Ucarturk N, Eur J Med Chem,200;, 39, 291. [10] Shah D I, Sharma M, Bansal Y, Bansal G& Singh M, Eur J Med Chem, 2008,43,1808.

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Publication Date

9/28/2026

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Review Rounds: 2

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