“…The characteristic resonances at the 23 and 37 ppm chemical shifts were not seen, which suggested that any 1-(2-hydroxyethyl)-1,4-dithianium formed and reacted quickly. An additional mechanism for the formation of 1,4-dithiane from sulfur mustard is via the intermediates H-H (45, 44, 43, 38, 35, 28 ppm), Q (43, 34, 32 ppm), and S(CH 2 CH 2 ) 2 S + CH 2 CH 2 Cl, 1-(2-chloroethyl)-1,4-dithianium (38, 37, 43, 23 ppm) (Scheme 6) [28]. The characteristic resonances for the S(CH 2 CH 2 ) 2 S + CH 2 CH 2 Cl at the 23 and 38 ppm chemical shifts were not seen, thus any formed would have reacted quickly.…”