【摘要】：正β-Amino carbonyl compounds are versatile intermediates for a large number of organic compounds and the derivatives of ferrocene have being attracted the attention of scientists all over the world because of their numerous applications in chemical sensing, asymmetric catalysis, material science and medical chemistry. As a part of program aiming to the synthesis of potential biological or pharmacological active compounds and with the increasing interest of our group in efficient, economic and environmentally friendly reactions, now we have searched an optimized route to 1-ferroceny1-3-amino carbonyl compounds via Michael-type reaction of amines to ferrocenylenones by being ground under solvent-free and catalyst-free conditions at room temperature.