Multistep flow synthesis of vinyl azides and their use in the copper-catalyzed huisgen-type cycloaddition under inductive-heating conditions

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Abstract

The multistep flow synthesis of vinyl azides and their application in the synthesis of vinyltriazoles is reported. The synthesis relies on a stable polymer-bound equivalent of iodine azide that serves to carry out 1,2-functionalization of alkenes in a telescope flow protocol. The intermediate 2-iodo azides are subjected to a DBU-mediated polymer-supported elimination step yielding vinyl azides in good yield. The third step involves the formation of vinyl triazoles by a copper-catalyzed Huisgen-"click" cycloaddition. The required heat is generated by electromagnetic induction based on copper. Copper serves both as heatable as well as catalytically active packed-bed material inside the flow reactor. © 2011 Kupracz et al; licensee Beilstein-Institut. License and terms: see end of document.

Figures

  • Table 1: Azido iodination of alkenes 2a–f under flow conditions with polymer-bound bisazido iodate(I) complex 5.
  • Table 2: Optimization of the elimination protocol and formation of vinyl azide 4a under batch conditions (entries 1–7) and as a flow protocol (entry 8).
  • Table 3: Optimization of the reaction of vinyl azide 4b in the inductively heated (IH) copper-catalyzed Huisgen-type cycloaddition.

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CITATION STYLE

APA

Kupracz, L., Hartwig, J., Wegner, J., Ceylan, S., & Kirschning, A. (2011). Multistep flow synthesis of vinyl azides and their use in the copper-catalyzed huisgen-type cycloaddition under inductive-heating conditions. Beilstein Journal of Organic Chemistry, 7, 1441–1448. https://doi.org/10.3762/bjoc.7.168

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