The unsubstituted 1, 2, 5-trithiepin (1) has been synthesized from the known 1, 2, 5- trithiepane (6) through two consecutive Pummerer rearrangements. Proton and carbon NMR spectra were completely analyzed, assigned, and correlated. The protons in 1 are shifted downfield by Δδ= 0.57 ppm for H3/H7 (δ= 6.57 ppm) and by 1.10 ppm for H4/H6 (δ= 7.24 ppm) relative to the 6, 7-dihydro-1, 2, 5-trithiepin (7). These downfield shifts are ...