132331-08-9Relevant academic research and scientific papers
Effect of structural factors and solvent nature in bromination of anilines
Bagmanov
experimental part, p. 1570 - 1576 (2011/06/20)
Reaction of electrophilic bromination of aniline containing various ortho, meta, and para substituents in the aromatic ring was studied. The optimal conditions for synthesis of mono-, di-, tri-, and tetrabromo derivatives of aniline and brominated analog of Aniline Black were found.
Regioselective, photochemical bromination of aromatic compounds using N-bromosuccinimide
Chhattise, Prakash K.,Ramaswamy,Waghmode, Suresh B.
, p. 189 - 194 (2008/03/30)
Regioselective nuclear bromination of aromatic compounds is investigated with N-bromosuccinimide as the brominating agent under UV irradiation to afford the corresponding brominated compounds. The reaction proceeds at ambient temperature (30 ± 2 °C) without any catalyst. In most of the reactions, regioselectively mono-brominated products are obtained in good to high yields. The conversion and selectivity for bromination depend on the nature of the substituent on the aromatic ring.
Photoreaction of nitrobenzenes with hydrobromic acid
McIntyre, Brian P.,Coleman, Brian D.,Wubbels, Gene G.
, p. 7709 - 7711 (2007/10/03)
Nitrobenzene and three derivatives (3-CO2H, 3-OH, and 4-OH) give tribromoanilines when irradiated in hydrobromic acid.
Solid-state Nuclear Bromination of Some Phenols by N-Bromosuccinimide
Goud, B. Satish,Desiraju, Gautam R.
, p. 244 - 245 (2007/10/03)
Treatment of crystalline dimethylphenols and hydroquinones with N-bromosuccinimide leads rapidly and regioselectively to ring-substituted products.
