1-Methyl-1H-imidazol-3-ium 2,3,4,5,6-pentafluorophenolate [mim]C6F5O as a novel nano ionic liquid was designed, synthesized and characterized by using various techniques such as Fourier transform spectroscopy infrared (FT-IR), nuclear magnetic resonance (NMR), x-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive x-ray spectroscopy (EDX), thermal gravimetric analysis (TGA), derivative thermal gravimetric (DTG) and elemental analysis (CHN). The described nano perfluoro ionic liquid was used as an efficient catalyst in the synthesis of 2-amino-4,5-dihydropyrano[3,2-c]chromene, 3-amino-1H-benzo[f]chromene and 2-amino-4H-chromene derivatives under mild and solvent-free conditions. Short reaction times, good yields of products, easy work-up are the major advantages of this work. پرونده مقاله

Silica Vanadic Acid, SVA, (oxo-vanadium has been supported on silica) as a dual Lewis and Bronsted acid ability was prepared and efficiently catalyzed one-pot multi-component condensation of enolizable ketones or alkyl acetoacetates with aromatic aldehydes, acetonitrile and acetyl chloride. The described reaction was produced β-acetamido ketone or ester derivatives in high to excellent yields in relatively short reaction times in heterogeneous catalytic system at room temperature. Other advantages of this method is applicable at large scales without significant loss of the yields. In addition, this method is superior to reported methods, for the synthesis of β-acetamido ketone or ester derivatives. پرونده مقاله

Friedel–Crafts synthesis of triarylmethanes over 3-methyl-1-sulfonic acid imidazolium tetrachloroaluminate under green conditions:In this work, Friedel–Crafts (FC) alkylation of various arenes with aromatic aldehydes catalyzed by 3-methyl-1-sulfonic acid imidazoliumtetrachloroaluminate {[Msim]AlCl4}, as a green catalyst, to prepare triarylmethanes (TAMs) has been carried out. Some aromatic aldehydes were reacted with arenes containing electron-donor substitutions such as anisole, veratrole, phenols, indole and 2-naphtole under solvent-free conditions. The catalyst was recovered and reused successfully for four times. Simple methodology, easy work up, solvent-free condition and excellent yields are some advantages of this work.The promising points for the presented method are high yield, green reaction profile, easier work up and simplicity which make it a useful process for the preparation of various triarylmethanes پرونده مقاله

1,1’-(Ethane-1,2-diyl)dipyridinium bistribromide (EDPBT) was used as a chemoselective and effective organocatalyst for the silylation of hydroxyl groups as well as desilylation of trimethylsilyl ethers under mild conditions at room temperature with good to excellent yields. پرونده مقاله