Schlosser, ManfredCastagnetti, E.2006-03-032006-03-032006-03-03200110.1002/1099-0690(200111)2001:21%3C3991::AID-EJOC3991%3E3.0.CO;2-Jhttps://infoscience.epfl.ch/handle/20.500.14299/226978Upon treatment of 1-bromo-2-(trifluoromethoxy)benzene with lithium diisopropylamide (LDA) at -100 DegC, 3-bromo-2-(trifluoromethoxy)phenyllithium is generated. It can be trapped as such, but isomerizes to afford 2-bromo-6-(trifluoromethoxy)phenyllithium when the temp. is raised to -75 DegC. The latter intermediate can be directly obtained from 1-bromo-3-(trifluoromethoxy)benzene. 1-Bromo-4-(trifluoromethoxy)benzene gives 5-bromo-2-(trifluoromethoxy)phenyllithium at -100 DegC, but at -75 DegC it slowly eliminates lithium bromide, thus setting free 1,2-dehydro-4-(trifluoromethoxy)benzene. In the same way, 1,2-dehydro-3-(trifluoromethoxy)benzene can be generated from 1-bromo-3-(trifluoromethoxy)benzene. Both arynes can be intercepted in situ with furan. The resulting [4+2] cycloadducts can be reduced with zinc powder, giving 1- and 2-(trifluoromethoxy)naphthalenes, they may be submitted to acid-catalyzed isomerization to produce trifluoromethoxy-1-naphthols, or they may be brominated to afford vic-dibromo derivs. Base-promoted dehydrobromination of the latter compds. produces 2- or 3-bromo-1,4-epoxy-1,4-dihydro-5- or -6-(trifluoromethoxy)naphthalenes, which undergo regioselective ring-opening in acidic media and halogen/metal exchange when treated with butyllithium. [on SciFinder (R)]Alkynes; Aromatic hydrocarbons Role: RCT (Reactant)SPN (Synthetic preparation)PREP (Preparation)RACT (Reactant or reagent) (arynes; prepn. of 12-didehydro-3- or -4-(trifluoromethoxy)benzene and its conversion to trifluoromethoxynaphthalenes)bromotrifluoromethoxybenzene lithiation trapping furan; benzene bromotrifluoromethoxy lithiation trapping furan; epoxynaphthalene prepn ring cleavage bromination; naphthol trifluoromethoxy prepn; naphthalenecarboxylic acid trifluoromethoxy prepntext::journal::journal article::research article