Catalyst-free thiophosphorylation of in situ formed ortho -quinone methides.

A metal-, chloride reagent and base-free thiophosphorylation reaction of in situ formed ortho -quinone methide ( o -QM) to synthesize functionalized thiophosphates has been developed. The reaction is an atom-economical process, producing water as the sole byproduct. (EtO) 2 P(O)SH functions as both a Brønsted acid and nucleophilic thiolate to produce the o -QM intermediate and the thiophosphate product, respectively. The aza o -QMs were also successfully thiophosphorylated in the presence of catalytic TsOH to form sulfonamido thiophosphates.