As a natural-based catalyst, nano-Fe3O4@dextrin/Si(CH2)3/DABCO was fabricated and characterized with different analytical methods such as field emission scanning electron microscopy, X-ray diffraction, Fourier-transform infrared spectroscopy, X-ray mapping, energy-dispersive X-ray spectroscopy, thermogravimetric analysis, and vibrating sample magnetometer. The mentioned new natural magnetic nanocatalyst was employed for the three-component synthesis of tetrahydrobenzo[b]pyrans and spirooxindoles from aromatic aldehyde […]
A convenient, rapid, and one-pot method for the synthesis of azo dyes has been developed. In this protocol, diazotization reagent (ArN2+ -CrO3–SiO2) was prepared via grinding of aromatic amines, NaNO2, wet SiO2 and nano silica chromic acid (Nano-SCA) without solvent at room temperature. The obtained diazotization reagent was sufficiently stable to be kept at room […]
Nano-silica supported boron trifluoride (BF3.SiO2) is an efficient, reusable and eco-friendly catalyst for chemoselective thioacetalization of aldehydes and ketones. So, this catalyst was applied for transthioacetalization of acetals and acylals into their corresponding 1,3-dithiolanes or 1,3-dithianes in good to excellent yields. The reactions were carried out at room temperature under solvent free and grinding conditions […]
Two simple protocols for the synthesis of three-component condensation reaction of an aldehyde, β-ketoester and urea or thiourea to obtain the 3, 4-dihydropyrimidin-2(1H)-ones (thiones) using nano silica phosphoric acid are reported. Short reaction times, high yields, reusability of catalyst and easy workup are some advantages of these protocols.
Silica supported phosphorus pentoxide (P2O5·SiO2) is an efficient catalyst for synthesis of 1,3,5-substituted pyrazoles via the condensation of 1,3-diketones and hydrazines. Simplicity of procedure, mild condition, being solvent-free, high yields, and easy workup are some advantages of this protocol.
An one-pot method has been developed for the synthesis of azo dyes via sequential diazotization–diazo coupling of aromatic amines with coupling agents at room temperature in the presence of Bi(NO3)3. 5H2O. Short reaction times, high yields, a clean process, simple methodology, easy work-up and green conditions are advantages of this protocol.
A convenient and efficient direct protocol for the preparation of antibacterial azo dyes by the reaction of 2-naphthol with aromatic amines in the presence of catalytic amount of N-methyl-2-pyrrolidonium hydrogen sulfate ([H-NMP]HSO4) was carried out under solvent free conditions. This method has some advantages such as: easy work-up and easy separation of catalyst from the […]
A highly efficient procedure for the preparation of N,N’-alkylidenebisamides in the presence of BF3.SiO2 as a catalyst is described. N,N’-alkylidenebisamides have been prepared via one-pot three-component condensation reaction of various aldehydes and amides. All of the reactions proceeded in high yields and in moderately short reaction times.
A convenient, one-pot method for the synthesis of diazonium salt has been developed by the sequential diazotization of aromatic amines with NaNO2, polymer- supported periodic acid (PPIA) and 2-naphthole under solvent-free conditions at room temperature. By using this method, several types of aromatic amine, containing electron-withdrawing and electron-donating groups, were rapidly converted to the corresponding […]
[B(OH)3]0.78[B(OH)2(OSO3H)]0.22 or (BSA) was simply prepared by addition of chlorosulfonic acid to commercial boric acid at room temperature. This cheap and green solid acid was used as an efficient catalyst for synthesis of acylals from aldehydes under solvent-free conditions at room temperature.
