6533b827fe1ef96bd1286ed4

RESEARCH PRODUCT

ChemInform Abstract: Synthesis of a Tetraazido-Substituted 2-Tetrazene from 1,5- Cyclooctadiene and Iodine Azide.

Herbert MeierBernd RoseDieter Schollmeyer

subject

chemistry.chemical_compoundchemistryCycloocteneTetrazene15-Cyclooctadienechemistry.chemical_elementHydrochloric acidGeneral MedicineAzideNonaneIodineMedicinal chemistry

description

In contrast to the addition of iodine azide to cyclooctene (1) or 1,3-cyclooctadiene (5), its reaction with 1,5-cyclooctadiene (12) leads mainly to the surprisingly stable tetraazido-substituted 2-tetrazene 14 The structure of this was established by 15N-NMR studies and an X-ray structural analysis. Treatment of 14 with hydrochloric acid yields the diazido-substituted 9-azabicyclo[3.3.1]nonane 20.

https://doi.org/10.1002/chin.199728117