A General Copper-Catalyzed Vinylic Halogen Exchange Reaction
journal contributionposted on 31.03.2016 by Antoine Nitelet, Gwilherm Evano
Any type of content formally published in an academic journal, usually following a peer-review process.
An efficient and general system for the halogen exchange reaction in alkenyl halides has been developed. Upon reaction with catalytic amounts of copper iodide and trans-N,N′-dimethylcyclohexane-1,2-diamine in the presence of tetramethylammonium chloride or bromide, a wide range of easily accessible alkenyl iodides can be smoothly transformed to their far less available chlorinated and brominated derivatives in excellent yields and with full retention of the double bond geometry. This reaction also enables the chlorination of bromoalkenes and could be extended to the use of gem-dibromoalkenes.