Abstract
Electrooxidation strategies for synthesizing readily oxidizable products face notable challenges, especially when the oxidation potential of the products is lower than that of the reactants or when high current densities are necessary. The electrooxidation synthesis of trivalent organophosphorus compounds (OPCs (III)) from white phosphorus (P(4)) has demonstrated potential but is hindered by selectivity issues due to over-oxidation. Herein, we report a tandem electro-thermal synthesis pathway that addresses these challenges in producing OPCs (III) from P(4). The process begins with an electrooxidation step that generates a stable trivalent phosphorus transfer reagent, then thermochemically converted into various high-value OPCs (III). Utilizing hexafluoroisopropanol (HFIP) as the nucleophile and optimizing a tetrabutylammonium iodide (TBAI)-4-dimethylaminopyridine (DMAP)-adduct catalytic system, we developed an efficient electrophilic phosphorus transfer reagent via electrosynthesis. The adduct facilitates the oxidation of P(4) and enhances the nucleophilicity of HFIP, thereby improving the electrooxidation process. This approach supports high current density, scales up to the hundred-gram level without yield loss, and remains compatible with fluctuating green electricity.