A novel monomer with two N‐phenylimide activating groups for the preparation of poly(aryl ether)s was investigated. A poly(aryl ether) was prepared by nucleophilic halide displacement from an aromatic dihalide monomer containing two N‐phenylimide groups by sodium salts of bisphenol A. The monomers and the resulting polymer were characterized by FT‐IR and 1H NMR spectroscopy, elemental analysis and differential scanning calorimetry (DSC). The prepared polymer with a molecular weight of 6 300 and a polydispersity of 1.37 determined by GPC is readily soluble in polar aprotic solvents, e. g. dimethylformamide (DMF), dimethylacetamide (DMAc), dimethylsulfoxide (DMSO), and N‐methyl‐2‐pyrrolidone (NMP). Despite the low molecular weight the polymer is thermally stable up to 390°C and has a glass transition temperature of 218°C which is identical to that of ULTEM® poly(ether imide).