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Published on: November 9, 2019
Hexamethylbenzene elimination enables the generation of transient, sterically unhindered multiply bonded boron
Chonghe Zhang1, Philipp Dabringhaus1, Bi Youan E Tra1
1Department of Chemistry, Massachusetts Institute of Technology Cambridge Massachusetts 02139 USA ccummins@mit.edu gilliard@mit.edu.
Abstract:
We present a method for the generation of boron-containing unsaturated small molecules via hexamethylbenzene elimination. The fragmentation precursors are obtained through bond insertion into phenyl boranorbornadiene (PhB(C6Me6), 1). Compound 1 undergoes 1,1-insertion with 2,6-xylyl isocyanide, affording a boron-doped bicyclo[2.2.2]octa-2,5-diene 2. Heating 2 in toluene results in the formation of a base-stabilized boraketenimine PhB(CNxyl)2 (i.e., borylene diisocyanide) as an intermediate via retro-Diels-Alder reaction. Surprisingly, PhB(CNxyl)2 dimerizes to give a boron-doped 6-membered ring (PhB)2C4(CNxyl)64. The reaction of 1 with trimethylamine N-oxide and phenyl azide yields triphenyl boroxine and a BN4 ring, respectively, implying the involvement of transient oxoborane (PhB[triple bond, length as m-dash]O) and iminoborane intermediates (PhB[triple bond, length as m-dash]NPh), respectively. Furthermore, boranorbornadiene also undergoes 2,3-insertion with mesityl isocyanate (MesNCO), affording a fused 6/5-membered heterocycle 11. This insertion profile is analogous to the insertion of phenyl azide into 1.
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