Decarboxylation of Hydroxybenzoic Acids to Phenol Via Deep Eutectic Solvents

Abstract

The development of greener and more sustainable synthesis processes for manufacturing commodity chemicals is of great importance. The majority of current phenol production methods involve harsh reaction conditions with high energy consumption, causing severe environmental pollution. In this study, we present a novel approach for the decarboxylation of hydroxybenzoic acids (HBAs) to phenol using a choline chloride-urea (ChCl-urea) deep eutectic solvent (DES). Our study reveals the remarkable dual performance of ChCl-urea both as a catalyst and solvent for the decarboxylation of HBA, resulting in a high phenol yield (94 mol %) under mild reaction conditions. The proposed reaction pathway, established through a combination of experiments and computational simulations, enhances our understanding of this process. The recyclability of the DES system during decarboxylation was also assessed. Our findings demonstrate that the integration of DES into conventional chemical processes can pave the way for sustainable manufacturing, exemplifying a novel approach for producing phenol from abundant natural resources using designer solvents. A greener deep eutectic solvent (DES) enables the development of a sustainable phenol production process from naturally abundant resources. The choline chloride-urea DES catalyzes the conversion of hydroxybenzoic acids into phenol under mild conditions, achieving high yield and recyclability. This novel approach exemplifies an environmentally friendly method for chemical manufacturing. image