Thermally accelerated Heck reaction under direct mechanocatalysis using palladium milling balls
Johanna Templ1, Suhmi Hwang1, Tino Schwemin1
1Ruhr Universität Bochum, Inorganic Chemistry I Universitätsstraße 150 44801 Bochum Germany johanna.templ@tuwien.ac.at lars.borchardt@rub.de.
None:
We present a direct mechanocatalytic approach for the Mizoroki-Heck coupling of aryl iodides with olefins using palladium milling balls as catalyst under elevated temperatures in a ball milling reactor. The high chemoselectivity for C(sp2)-I bonds ensures a single product when employing multi-halogenated arenes. Additionally, a one-pot Wittig olefination/Heck cross-coupling enables direct access to stilbene derivatives from aldehydes and aryl iodides without intermediate isolation.
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