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Benzofurazans bromination

Benzofurazan (benz-1,2,5-oxadiazole) reacted with bromine by addition to give a4,5,6,7-tetrabromo adduct. Bromine in hydrobromic acid solution 4-brominated both 5-methyl- and 5-bromo-benzofurazans (74JHC8I3). When 4,7-dinitrobenzofurazan was treated with ammonium chloride in refluxing acetic acid, nucleophilic displacement gave rise to the 4-chloro-7-nitro derivative (83URP1004375). Naphtho[l, 2-c]furazans (42) are mainly 4-halogenated, but there is minor substitution in the 8-position (73CHE1331). [Pg.277]


See other pages where Benzofurazans bromination is mentioned: [Pg.4]    [Pg.252]    [Pg.409]    [Pg.559]    [Pg.409]    [Pg.3]    [Pg.4]    [Pg.726]    [Pg.299]   
See also in sourсe #XX -- [ Pg.47 , Pg.227 ]




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