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Upstream product

• 55-21-0 benzamide 
• 100-52-7 benzaldehyde 
• 135-19-3 β-naphthol 
• 60-35-5 acetamide 
• 100-47-0 benzonitrile 
• 98-88-4 benzoyl chloride 

Relevant academic research and scientific papers

Nano silica sulfuric acid an efficient and recoverable heterogeneous catalyst for the preparation of amidoalkyl naphthols under solvent-free conditions

An efficient and green method has been developed for the synthesis of amidoalkyl naphthol derivatives through a one-pot threecomponent condensation of 2-naphthol, aldehydes, and amide in the presence of nano silica sulfuric acid as heterogeneous catalyst under solvent-free conditions. Taylor & Francis Group, LLC.

Zinc benzenesulfonate-promoted ecofriendly and efficient synthesis of 1-amidoalkyl-2-naphthols

A three-component, one-pot condensation of 2-naphthol, aldehydes, and amides catalyzed by zinc benzenesulfonate gives 1-amidoalkyl-2-naphthols in good yields at 80°C under solvent-free conditions. The catalytic activities of zinc benzenesulfoante and 12 o

Simple hydrothermal synthesis of sphere-like TiO2 nanoparticles and their functionalization with 1,4-butane sultone as a new heterogeneous catalyst

Abstract: For the first time, anatase TiO2 nanoparticles with high specific surface area have been synthesized by hydrothermal method using titanium (IV) ethoxide solution. Nanocrystalline titania-based sulfonic acid (nano-TiO2–Bu–SO

Graphite-supported perchloric acid (HClO4-C): An efficient and recyclable heterogeneous catalyst for the one-pot synthesis of amidoalkyl naphthols

An efficient and direct protocol for the preparation of amidoalkylnaphthols employing a multi-component, one-pot condensation reaction of 2-naphthol, aromatic aldehydes and acetamide or benzamide in the presence of graphite supported perchloric acid under

A simple and efficient procedure for the synthesis of amidoalkyl naphthols by p-TSA in solution or under solvent-free conditions

An efficient and direct procedure for the synthesis of amidoalkyl naphthols has been described that employs a three-component condensation reaction in one pot using aromatic aldehydes, β-naphthol and ureas or amides in the presence of p-toluene sulfonic acid in 1,2-dichloroethane at room temperature or under solvent-free conditions at elevated temperature. Georg Thieme Verlag Stuttgart.

Monometallic and bimetallic Cu-Ag MOF/MCM-41 composites: Structural characterization and catalytic activity

Monometallic and bimetallic MOF/MCM-41 composites (Cu, Ag and Cu-Ag) were synthesized via a solvothermal method. The synthesized composites were characterized by XRD, FTIR, SEM, EDX and BET surface area measurements. The acidity was determined through two

Physicochemical characterization and catalytic applications of MoO 3-ZrO2 composite oxides towards one pot synthesis of amidoalkyl naphthols

A series of MoO3-ZrO2 composite oxide catalysts were prepared by coprecipitation and impregnation methods and characterized by XRD, Raman, UV-Vis, TEM and sorptometric techniques. Characterization studies indicated the presence of te

Sulfonated polynaphthalene as an effective and reusable catalyst for the one-pot preparation of amidoalkyl naphthols: DFT and spectroscopic studies

Sulfonated polynaphthalene (S-PNP) as a carbon-based solid acid efficiently catalyzed the one-pot three-component synthesis of amidoalkyl naphthols. The three-component process of substituted aryl aldehydes, 2-naphthol, and amide (benzamide and acetamide)

Catalytic activity of dual metal cyanide complex in multi-component coupling reactions

Several dual metal cyanide catalysts were prepared from potassium ferrocyanide, metal chloride (where metal = Zn2+, Mn2+, Ni2+, Co2+, and Fe2+), t-butanol (complexing agent) and PEG-4000 (co-complexin

Silica supported methanesulfonic acid as an efficient and reusable heterogeneous catalyst for the synthesis of amidoalkyl naphthols

A green protocol for the preparation of amidoalkyl naphthols from three-component one-pot condensation of 2-naphthol, aldehydes, amides or urea in the presence of silica supported methanesulfonic acid under thermal solvent-free conditions has been describ