Solvent-free synthesis of 1-amidoalkyl-2-naphthol and 3-amino-1-phenyl-1 <i>H</i> benzo[ <i>f</i> ]chromene-2-carbonitrile derivatives by Fe ₃ O ₄ @enamine-B(OSO ₃ H) ₂ as an efficient and novel heterogeneous magnetic nanostructure catalyst

Abstract

Abstract A green procedure for the one-pot three-component synthesis of 1-amidoalkyl-2-naphthol and 3-amino-1-phenyl-1 H benzo[ f ]chromene-2-carbonitrile derivatives from the reaction of 2-naphtol, aldehydes, and malononitrile/acetamide in the presence of a catalytic amount of Fe 3 O 4 @enamine-B(OSO 3 H) 2 as an efficient and novel heterogeneous magnetic nanostructure catalyst is described. The catalyst was characterized using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), energy dispersive X-ray spectroscopy (EDX), and X-ray diffraction (XRD). These strategies possess some merits such as simple work-up method, easy preparation of the catalyst, short reaction times, good-to-high yields, and non-use of hazardous solvents during all steps of the reactions. Moreover, due to the magnetic nature of the catalyst, it was readily recovered by magnetic decantation and can be recycled at least six runs with no considerable decrease in catalytic activity.