Xanthene-1,8-dione derivatives are of significant interest in pharmacology and materials chemistry due to their biological and optical properties. However, their traditional synthesis often involves toxic catalysts or environmentally harmful solvents. We propose a novel eco-friendly approach for synthesizing these compounds using green reaction conditions, avoiding hazardous organic solvents and minimizing unwanted byproducts.

The synthesis is carried out via condensation between dimedone and various aldehydes in the presence of linear alkylbenzene sulfonic acid (LABSA) as a biodegradable and cost-effective phase-transfer catalyst and under alternative activation methods such as ultrasound irradiation. The reaction is optimized to maximize yield while reducing environmental impact. LABSA, functioning both as a Brønsted acid and surfactant, is proposed to facilitate a multicomponent cascade process involving Knoevenagel condensation, Michael addition, and intramolecular cyclization

Xanthene-1,8-dione derivatives are obtained in high yields (88%-90%) with excellent purity. The method offers significant advantages, including reduced reaction time, atom economy, and easy purification. The products are characterized by spectroscopy (NMR, IR, MS) and chromatographic analysis. In IR strong carbonyl stretching bands observed near ~1623–1634 cm⁻¹ are characteristic of two conjugated carbonyl groups at positions 1 and 8 of the xanthene core.

This green strategy provides a sustainable alternative to conventional protocols, aligning with the principles of green chemistry. It opens new possibilities for the eco-friendly synthesis of heterocycles valuable in pharmaceuticals and fine chemistry.