Paper
Synthesis, structure, and ambident alkylation reactions of 3-aryl-1-(tetrazol-5′-yl)triazenes
Published 1984 · R. N. Butler, Declan P. Shelly, V. C. Garvin
Journal of The Chemical Society-perkin Transactions 1
6
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Abstract
A series of 3-aryl-1-(tetrazol-5′-yl)triazenes was prepared by coupling tetrazole-5-diazonium ion with substituted anilines. The orientation of the ambident methylation reactions of the anion of these systems was investigated. 13C N.m.r. spectra of the mono- and di-methyl derivatives provided information on the preferred tautomeric structure of the parent triazenyltetrazole system.
3-aryl-1-(tetrazol-5′-yl)triazenes show promising potential for organic synthesis and a variety of ambident methylation reactions.
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