Herein, we report a direct amidation reaction of ferrocenyl/phenyl substituted β-chlorocinnamaldehyde in presence of a robust and chalcogen stabilized iron selenide carbonyl cluster Fe3Se2(CO)9. The amidation of vinylic Csp2-Cl and amides was established and Csp2-N bond formation was obtained at strongly feasible reaction conditions. The wide substrate scope of the reaction has been investigated for functionally different amides and β-chloro derivatives. The present method was found to be superior in terms of the time duration, substrate scope, and use of inexpensive metal. Moreover, 2 mol % of cluster Fe3Se2(CO)9 was found to be highly efficient to couple various substituted primary amides (aliphatic, hetero, aromatics) with β-chlorocinnamaldehyde in just 4 h under aerobic conditions. To the best of our minds, it is the first report where the α, β-unsaturated derivatives of ferrocene have been explored for direct amidation reaction.
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