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It is useful for organic synthesis of aromatic compounds. Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.
Biju M. Devassy.; S.B. Halligudi. Zirconia-supported heteropoly acids: Characterization and catalytic behavior in liquid-phase veratrole benzoylation.J. Catal. 2005, 236 (2),313-323.
Irene M. Matheson (née Davidson).;O. C. Musgrave.; C. J. Webster. Oxidation of veratrole by quinones. Chem. Commun. (London). 1965, (13), 278-279.
In contrast to 1,3-Dimethoxybenzene, A13380, direct dilithiation with n-BuLi + TMEDA is feasible, giving, after reaction with TMS chloride, the 3,6-disilyl derivative as the major product in 50-60% yield: J. Org. Chem., 49, 4657 (1984).
Gefahrenhinweise (EU): H227-H302
Combustible liquid. Harmful if swallowed.
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