Abstract

1,2-Dihalosilene is a hitherto unknown but potentially useful functionalizable compound for new silenes and silicon–carbon triply bonded species. We successfully generate 1,2-dibromosilene 1 by the reaction of tetrabromo derivative 2 with BuLi. The formation of 1 is confirmed by NMR studies and trapping experiments. Silene 1 survives under −80 °C, but 1 thermally isomerizes to silacyclohexane 6 via a 1,2-bromine shift to form bis(silyl)carbene 11 and the subsequent intramolecular C–H insertion.

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