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Bromo subs acetic acid

Halogenation of 2-quinoxalinone (60) in acetic acid gives the 7-sub-stituted product almost quantitatively bromine at 20° thus yields 95% of 7-bromo-2-quinoxalinone (61).72... [Pg.383]

Although electrophilic substitution reactions are possible with oxazoles, they are frequently accompanied by addition reactions, as in furan. The bromination of 4-methyl-2-phenyloxazole with bromine or A/-bromosuccinimide yields 5-bromo-4-methyl-2-phenyloxazole, and that of 2-methyl-5-phenyloxazole gives 4-bromo-2-methyl-5-phenyloxazole. Mercury(II) acetate in acetic acid acetoxymercurates 4-sub-stituted oxazoles in the 5-position, 5-substituted oxazoles in the 4-position, and 4,5-disubstituted oxazoles in the 2-position. The acetoxymercury group can be substituted by electrophiles, e.g. ... [Pg.124]


See other pages where Bromo subs acetic acid is mentioned: [Pg.293]    [Pg.357]    [Pg.803]    [Pg.609]    [Pg.571]    [Pg.397]    [Pg.339]   
See also in sourсe #XX -- [ Pg.124 ]




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