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Meisenheimer complexes from trinitrobenzene

Arylthiophenes are formed by reaction of 2-thienylcopper with iodoarenes (Scheme 182) (70ACS2379, 71ACS2428). A Meisenheimer complex (501) has been prepared from 2-thienylcopper and trinitrobenzene (71TL2713). [Pg.836]

The reaction of l,2-dichloro-4,5-dinitrobenzene with dilute aqueous sodium hydroxide results in substitution of a nitro-group by hydroxide. However, in hydroxide concentrations greater than 2 mol-dm", only the formation of monohydroxy- and dihydroxy-adducts (42) is observed, and acidification yields the original reactant. The cyanide adduct (43) of 1,3,5-trinitrobenzene has been observed by electrospray ionization mass spectrometry, using acetonitrile as the cyanide source. X-ray structures of the stable crystalline adducts formed from 4,6-dinitrobenzofiiroxan and dodecyl- and hexadecyl-amine have been reported. There has also been a report, related to the destruction of energetic materials, of Meisenheimer complex formation during the alkaline hydrolysis of 2,4,6-trinitrotoluene and 2,4-dinitroanisole. ... [Pg.227]


See other pages where Meisenheimer complexes from trinitrobenzene is mentioned: [Pg.299]    [Pg.158]    [Pg.240]    [Pg.306]    [Pg.158]    [Pg.240]    [Pg.158]    [Pg.391]    [Pg.88]   
See also in sourсe #XX -- [ Pg.95 , Pg.241 , Pg.242 ]




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