Abstract
A simple and efficient procedure for the preparation of silica-bonded propylpiperazine- N-sulfamic acid (SBPPSA) by the reaction of 3-piperazine- N-propylsilica (3-PNPS) and chlorosulfonic acid in chloroform is described. Silica-bonded propylpiperazine- N-sulfamic acid is employed as a recyclable catalyst for the synthesis of highly substituted imidazoles from the reaction of benzil, aromatic aldehydes, ammonium acetate and amines under solvent-free conditions. The heterogeneous catalyst was recycled for five runs upon the reaction of benzil, 4-methylbenzaldehyde, benzylamine, and ammonium acetate without losing its catalytic activity.
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