Atom economic in situ domino N-alkylation reactions of triethylamine/ammonia with 2-(hydroxymethyl)quinolin-8-ol (HL-OH) assisted by FeSO4 center dot 7H(2)O were realized under mild solvothermal conditions at 120 degrees C in acetonitrile. The resulting tripodal 2,2',2 ''-[nitrilotris (methylene)] tris(quinolin-8-ol) (H3L3-N) forms a linear trimer [Fe-3(L-3-N)(2)] (1). Electrospray ionization mass spectrometry of the reaction solution provides evidence for the intermediates of three steps, while crystallography and X-ray photoelectron spectroscopy characterize the trimer. Shortening the time of the reaction allowed for the organic intermediates to be isolated, which led to a proposed mechanism. The method provides a facile way to produce symmetric tertiary amine from widely used NEt3 and NH3. The results represent an example of the in situ Fe2+-catalyzed domino reaction in which Fe2+ is coordinated by the generated ligands and is involved in each step until the final cluster 1.