Mode of Attack of Atomic Carbon on Benzene Rings

Abstract

Reaction of arc generated carbon atoms with tert-butylbenzene, 4, gives 3-methyl-3-phenyl-1-butene, 5, and 1,1-dimethylindane, 6. Labeling studies and isotope effects demonstrate that 5 results from an insertion into a methyl C−H bond followed by 1,2 hydrogen shift while 6 arises from initial ortho C−H insertion followed by intramolecular insertion into a methyl C−H bond. When fluoroboric acid is added to the 77 K matrix of 4 + C, tert-butyltropylium fluoroborate, 18, is formed. Labeling studies indicate that 18 results from initial insertion of C into meta and para C−H bonds of 4 followed by ring expansion to cycloheptatetraenes which are subsequently protonated. The reaction of C with benzene gives similar results, indicating that initial C−H insertion is the preferred mode of attack of atomic carbon on benzene rings.