This report details the study of the nucleophilic substitution of 1-benzyl-3,5-dibromo-lH-1,2,4-triazole. A variety of nucleophiles have been studied to date. The nucleophiles studied primarily fall into the categories of Phosphorous, Oxygen and Sul fur species. Some of the initially formed substitution products are thermally unstable and undergo unique rearrangements. The report describes the physical properties, 1H NMR, 13c NMR, IR and Mass spectra for all of the synthesized compounds. Possible mechanistic pathways are presented for the formation of the prepared compounds. Recommendations are made in order to suggest future research opportunities in this area.
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Gupton, John T.
Master of Science (M.S.)
College of Arts and Sciences
Length of Campus-only Access
Masters Thesis (Open Access)
Orlando (Main) Campus
Arts and Sciences -- Dissertations, Academic; Dissertations, Academic -- Arts and Sciences
Fivush, Adam Michael, "New synthetic transformations of 1-benzyl, 3,5-dibromo, 1h-1,2,4-triazole /c" (1988). Retrospective Theses and Dissertations. 4280.