Abstract
Indium trichloride promotes the chlorination of terminal olefins in the presence of sodium hypochlorite with good results. Carvone was chosen as a model compound to examine some of the general features of this reaction, such as stoichiometry, temperature, reaction time and product conversion. Treatment of β-pinene with sodium hypochlorite in the presence of indium trichloride resulted in a facile rearrangement to selectively yield perillyl chloride, which is an important precursor for C-7 oxygenated limonenes. ©2006 Sociedade Brasileira de Química.
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Pisoni, D. S., Gamba, D., Fonseca, C. V., Da Costa, J. S., Petzhold, C. L., De Oliveira, E. R., & Ceschi, M. A. (2006). InCl3NaClO: A reagent for allylic chlorination of terminal olefins. Journal of the Brazilian Chemical Society, 17(2), 321–327. https://doi.org/10.1590/s0103-50532006000200015
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