The direct synthesis of propylene carbonate (PC) through a tandem epoxidation-cycloaddition reaction from propylene and CO 2 is considered a highly promising industrial process due to its streamlined procedure, atomic efficiency, costeffectiveness, and inherent safety. In this work, we investigated the thermal stability of oxidants critical for the tandem epoxidationcycloaddition reaction, aiming to determine the optimal oxidant between hydrogen peroxide (H 2 O 2 ) and cumene hydroperoxide (CHP). This evaluation is particularly significant given the tendency of oxidants to decompose at a higher temperatures required for the cycloaddition reaction. Our findings indicate that CHP is a superior oxidant for facilitating the tandem epoxidationcycloaddition coupling at high reaction temperatures, due to its higher decomposition temperature (122 °C) compared to H 2 O 2 (40 °C). Furthermore, we present for the first time a one-pot synthesis of PC through a tandem epoxidation-cycloaddition reaction using CHP as the oxidant for the epoxidation step, achieving PC yield of 79.8%. Additionally, a plausible reaction mechanism for this tandem epoxidation-cycloaddition reaction of propylene and CO 2 is proposed, based on experimental observations and supported by density functional theory (DFT) calculations. Specifically, DFT calculations reveal that the synergistic effect between hydroxyl groups and Br − promotes the ring-opening of propylene oxide (PO).