An　electrochemically　promoted　coupling　of　benzoxazoles　and　amines　has　been　developed,　leading　directly　to　the　formation　of　2-aminobenzoxazoles.　The　chemistry　utilizes　catalytic　quantities　of　a　tetraalkylammonium　halide　redox　catalyst　and　is　carried　out　under　constant　current　conditions　in　a　simple　undivided　cell.　The　use　of　excess　chemical　oxidant　or　large　amounts　of　supporting　electrolyte　is　avoided.　This　greatly　simplifies　the　workup　and　isolation　process　and　leads　to　a　reduction　in　waste.