Arene Cyclopropanation

  • Author: Li Grundl
  • Published: 17 July 2017
  • Copyright: Wiley-VCH Verlag GmbH & Co. KGaA
  • Source / Publisher: Advanced Synthesis & Catalysis/Wiley-VCH
thumbnail image: Arene Cyclopropanation

Cycloheptatrienes and norcaradienes are useful building blocks in organic synthesis. They can be efficiently synthesized from transition-metal-catalyzed Buchner reactions and arene cyclopropanations using diazo compounds as carbene sources. Recently, alkyl diazomethanes are found to be effective carbene sources with good diastereo- and chemo-selectivity, but the related studies are still rare.

Chi-Ming Che, The University of Hong Kong, China, and colleagues have developed a method to synthesize cycloheptatriene and norcaradiene derivatives from aniline derived N-tosylhydrozones using cobalt-porphyrin as a catalyst and K2CO3 as a base in dioxane at 105 °C. The reactions gave cycloheptatrienes in good yields. Interestingly, when 2-naphthylamine derivatives were used, the reactions stopped at the cyclopropanation stage to give a tetracyclic product (see pictured).

The reactions are found to be highly regioselective and the cyclopropanation/tautomerization step might not be the rate-determining step. In case of 2-naphthylamine derivatives, the electrocyclic ring opening might be kinetically and thermodynamically disfavored by a concomitant dearomatization. The tetracyclic cyclopropane products can be further converted to other N-heterocycles.


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