Ligand-Promoted Nickel-Catalyzed -Selective Carboxylation of Anisoles.

It has always been a challenge in free radical chemistry to control site selectivity during the reaction of free radicals with aromatic rings. Herein, we report the site-selective carboxylation of anisoles through the direct reaction of the bromoform radical with a benzene ring at the position under the assistance of 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline with nickel(II) as the catalyst. A wide variety of anisoles were compatible, leading to -carboxylated products in moderate to good yields. A preliminary mechanistic study suggested that the Ni(II) complex coordinates with the methoxyl group of the aromatic ring, which may have increased the steric hindrance at the and positions, while this weak interaction reduces the aromaticity of the aromatic ring, affording an activated phenyl ring, thereby leading to highly -selective carboxylation.