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Heating a mixture of 2,5-dimethyl-3-hexyne-2,5-diol(3a) with elemental sulfur in benzene at 190-200 "C in an autoclave affords 3.6-dimethylthieno[3,2-blthiophene (5a) in 26% yield. The reaction provides a practical one-pot synthesis of several gram quantities of 5a, even if the yield is moderate, since 3a is commercially available and inexpensive. The reaction proceeds via 2,5-dimethyl-1.5-hexadiene-3-yne (4a) as one of probable intermediates, which is produced by dehydration of 3a. Addition of p-toluenesulfonic acid promotes the dehydration of 3a and thus can lower the reaction tempera-.In addition, the reaction of 4a, prepared from 3a independently, with sulfur affords 5a in a somewhat improved yield (33%). The reaction of 3a with elemental selenium also provides a one-pot synthesis of 3,6-dimethylselenolo[3,2-blselenophene (9a) in 16% yield. Reactions of some other acetylenic diols with elemental sulfur and selenium are also described.14. F. Woods andL. H. S c h w m a n ,

1994organo-selenium compounds, nonmetal heterocycles organo-selenium compounds, nonmetal heterocycles S 0137 -188A One-Pot Synthesis of Substituted Thieno(3,2-b)thiophenes and Selenolo(3,2-b)selenophenes.-Heating the hexynediols (I) with elemental sulfur or selenium yields directly the fused heterocycles (II) and (III) in low yield. -(CHOI, K. S.; SAWADA, K.; DONG, H.; HOSHINO, M.; NAKAYAMA, J.; Heterocycles 38 (1994)