Abstract
A new efficient protocol for the ortho‐methylation of benzamides with DTBP has been developed via Ni(II)‐catalyzed C–H activation directed by 8‐aminoquinoline. This method is performed under base‐free, ligand‐free conditions and utilizes cheap and commercially available reagents. Moreover, the by‐product acetone derived from DTBP does not affect the purification of the product.
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