CYCLOCONDENSATION OF DICHLOROETHENES WITH ALKANEDICHALCOGENOLATES IN THE HYDRAZINE HYDRATE – ALKALI SYSTEM. THE SYNTHESIS OF DIHYDRODITHIINE AND TRIHYDRODICHALCOGENEPINES
Keywords:
dihaloethenes, 6,7-dihydro-5H-1,4-diselenepine, 6,7-dihydro-5H-1,4-dithiepine, 5,6-dihydro-1,4-dithiine, hydrazine hydrate – alkali system, mass spectraAbstract
Vinylidene chloride and 1,2-dichloroethene (a 1.3:1 mixture of Z- and E-isomers) reacted with 1,2-ethanedithiolate or 1,3-propanedichalcogenolates (S, Se) under mild conditions to form cyclocondensation products. Alkanedichalcogenolates were generated from the corresponding oligomeric dichalcogenides by the action of a hydrazine hydrate – alkali reducing system and were used without isolation from the reaction mixture. 1,3-Propaneditellurolate did not form the corresponding heterocycle, regenerating poly(trimethylene ditelluride) during the reaction.
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Published
2024-12-13
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Short Communications