Nickel/aluminium oxide as a sustainable and cost-effective catalyst for the Sonogashira coupling reaction

In our study, we report a cost-effective and sustainable Sonogashira coupling reaction with Nickel supported on alumina (Ni/Al 2 O 3 ) as a palladium-free catalyst. The procedure effectively couples phenylacetylene and 2-ethynylpyridine with various aryl iodides under optimized conditions and provides a greener route by reducing hazardous waste , cost-effectiveness, and eliminating toxic palladium catalysts. The simplicity of catalyst preparation and reusability of the catalyst make the procedure amenable to large-scale applications in keeping with green chemistry principles. • A straightforward and efficient method for synthesizing Ni/Al 2 O 3 catalysts under mild conditions. • Demonstration of high catalytic activity and excellent yields (up to 90 %) with low catalyst loading (5 mol%). • Recyclability of the catalyst over multiple cycles with minimal loss of efficiency. • A broad substrate scope, including heteroaryl and functionalized aryl halides, under optimized green reaction conditions.

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Publication Details

Journal
Tetrahedron
Published
2025-04-24
DOI
https://doi.org/10.1016/j.tet.2025.134678
Citations
3
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
2.81
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article

Nickel/aluminium oxide as a sustainable and cost-effective catalyst for the Sonogashira coupling reaction

Manjunath S. Lokolkar, Sai Srinivas Ponugoti, Shreerang V. Joshi, Bhalchandra Mahadeo Bhanage et al.
3 citations
Tetrahedron
Catalytic Cross-Coupling Reactions
2.81
article

Nickel/aluminium oxide as a sustainable and cost-effective catalyst for the Sonogashira coupling reaction

Manjunath S. Lokolkar, Sai Srinivas Ponugoti, Shreerang V. Joshi, Bhalchandra Mahadeo Bhanage, Priyanka Rajesh Ugale, Priya C. Saroj
article en
3 citations

Abstract

In our study, we report a cost-effective and sustainable Sonogashira coupling reaction with Nickel supported on alumina (Ni/Al 2 O 3 ) as a palladium-free catalyst. The procedure effectively couples phenylacetylene and 2-ethynylpyridine with various aryl iodides under optimized conditions and provides a greener route by reducing hazardous waste , cost-effectiveness, and eliminating toxic palladium catalysts. The simplicity of catalyst preparation and reusability of the catalyst make the procedure amenable to large-scale applications in keeping with green chemistry principles. • A straightforward and efficient method for synthesizing Ni/Al 2 O 3 catalysts under mild conditions. • Demonstration of high catalytic activity and excellent yields (up to 90 %) with low catalyst loading (5 mol%). • Recyclability of the catalyst over multiple cycles with minimal loss of efficiency. • A broad substrate scope, including heteroaryl and functionalized aryl halides, under optimized green reaction conditions.

TetrahedronVol. 184
Institute of Chemical Technology (IN)
Responsible consumption and production
Openalex Percentile: Top 11%
Catalytic Cross-Coupling Reactions
2.81
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Nickel/aluminium oxide as a sustainable and cost-effective catalyst for the Sonogashira coupling reaction — Manjunath S. Lokolkar, Sai Srinivas Ponugoti, et al. · Tetrahedron (2025) | TGRS Research Map | TGRS