2-, 3-and 4-Methoxytoluene can be selectively metalated at an O-adjacent ortho position when butyllithium or tert-butyllithium in the presence of sodium (potassium) tert-butoxide or N, N, N′, N ″, N ″-pentamethyldiethylenetriamine are employed as reagents. In contrast, lithium diisopropylamide or lithium 2, 2, 6, 6-tetramethylpiperidide deprotonate the benzylic α-position of 2-and 3-methoxy-toluene exclusively and of 4-methoxytoluene preferentially. ...
[Higgins, Stanley D.; Thomas, Barry C. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1982 , p. 235 - 242]