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1.4- Dimethoxy-2,6-dimethylbenzene

The present method of preparation of 4,4 -dimethyl-l,l -biphenyl is that described by McKillop, Elsom, and Taylor 15 It has the particular advantages of high yield and manipulative simplicity and is, moreover, applicable to the synthesis of a variety of symmetrically substituted biaryls 3,3 - and 4,4 -Disubstituted and 3,3, 4,4 -tetrasubstituted 1,1 -biphenyls are readily piepared, but the reaction fails when applied to the synthesis of 2,2 -disubstituted-l,T biphenyls The submitters have effected the following conversions by the above procedure (starting aromatic bromide, product biphenyl, % yield) bromobenzene, biphenyl, 85,1 -bromo-4-methoxybenzene, 4,4 -dimethoxy-l, 1 -biphenyl, 99, 1 bromo 3 methylbenzene, 3,3 dimethyl-1,l -biphenyl, 85 4-bromo-l,2-dimethylbenzene, 3,3, 4,4 -tetramethyl-l,l -biphenyl, 76, l-bromo-4-chlorobenzene, 4,4 -dichloro-l,l -biphenyl, 73, l-bromo-4-fluorobenzene, 4,4 -difluoro-l,l -biphenyl, 73... [Pg.51]

In l,l,l,3,3,3-hexafluoropropan-2-ol, the reaction of l,4-dimethoxy-2,3-dimethylbenzene with a deficit of nitrogen dioxide gives a high concentration of the aromatic cation-radical, which lives long enough and can be detected spectroscopically. In the presence of excessive amounts of N02, this cation-radical decays rapidly giving the 5-nitro derivative of the starting compound (Eberson etal. 1996). [Pg.258]

ICS 205-930 = (3-tropanyl)-IH-indole-2-carboxylic acid ester DOM = 2,5-dimethoxy-4-dimethylbenzene ethamine... [Pg.137]

F,SCH, Methanesulfonic acid, trifluoro-iridium, manganese and rhenium complexes, 26 114, 115, 120 platinum complex, 26 126 OiFeCgH, Iron, acetyl dicarbonyl (if -cyclopentadienyl)-, 26 239 0,FeN2C2 Hll(, Iron, tricarbonylbis(2-isocy-ano-l,3-dimethylbenzene)-, 26 54 0.iMoNaCHH5-2 C4H ,02, Molybdate 1 -), tricarbonyl(T) -cyclopentadienyl)-sodium, compd. with 1,2-dimethoxy-ethane-(l 2), 26 343 0,NaWC H5-2 C4H ,02, Tungstate(l -), tricarbonyl(ris-cyclopentadienyl)-... [Pg.430]

Perfluoro(l,3-dimethylbenzene) and sodium methoxide yield, depending on the amount of the nucleophile used, l,2,4-trifluoro-6-methoxy-3,5-bis(trifluoromethyl)benzene (19) or 1,4-di-fluoro-2,6-dimethoxy-3,5-bis(trifluoromethyl)benzene (20).94... [Pg.398]


See other pages where 1.4- Dimethoxy-2,6-dimethylbenzene is mentioned: [Pg.411]    [Pg.21]    [Pg.80]    [Pg.411]    [Pg.411]    [Pg.430]    [Pg.1899]   
See also in sourсe #XX -- [ Pg.411 ]




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1.2- dimethylbenzene

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