Herein, a sustainable solid‐state procedure was employed for the synthesis of a water soluble molecule obtained d by linking hyaluronic acid to the hydrophobic quercetin (HA‐QCT). The micellar self‐aggregation of the developed conjugate suggested its employment as drug delivery nano‐system, considering the numerous biological activities of QCT. Indeed, the spectroscopic characterization (UV‐vis and FT‐IR) ensured that the QCT maintained its chemical integrity. In addition, a cytotoxicity test revealed that HA‐QCT could be employed as a biocompatible drug vehicle for pharmacological purposes. A preliminary colorimetric test also confirmed that QCT retained its anti‐oxidant activity