An efficient synthesis of the 1-hydroxy-2-(prop-2'-enyl)9-anthrone is described. Selective nitration of anthraquinone, reduction to the corresponding amine, diazotization and treatment by sulfuric acid solution afforded the 1-hydroxy-9,10-anthraquinone in good yield as the key intermediate. Reaction with allyl bromide/K2CO3 and subsequent selective reduction accompanie...

an efficient and environmentally benign   method for the synthesis of aryl iodides have been developed by diazotization of aromatic amines with nano2 and nanosilica periodic acid (nano-spia) as a green catalyst via grinding followed by a sandmeyer iodination by ki under solvent-free conditions at room temperature. the ensuing aryl diazonium salts supported on nano-spia were sufficiently stable ...

A sulfonated graphene catalyst was designed and tested in the acetylation of glycerol. The synthesized using graphite as starting material comprised three stages, which included: (i) synthesis oxide by means a modified Hummers method, (ii) reduction with ascorbic acid, (iii) functionalization sulfanilic acid situ diazotization. Structural, morphological chemical properties were characterized SE...

Five new 1-hydroxy-2-(1-alkyloxymethyl)-9,10-Anthraquinones (9a-e) have been prepared. Selective nitration of 2-methyl-9,10-anthraquinone, reduction to the corresponding amine, diazotization and treatment by sulfuric acid solution afforded the 1-hydroxy-2-methyl-9,10-anthraquinone in good yield as the key intermediate. Reaction with dimethylsulphate/K2CO3 and subsequen...

An efficient and environmentally benign   method for the synthesis of aryl iodides have been developed by diazotization of aromatic amines with NaNO2 and nanosilica periodic acid (nano-SPIA) as a green catalyst via grinding followed by a sandmeyer iodination by KI under solvent-free conditions at room temperature. The ensuing aryl diazonium salts supported on nano-SPIA were sufficiently stable ...

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 ...