| dc.contributor.author | Andrievsky, Alexander M. | |
| dc.contributor.author | Lomzakova, Vera I. | |
| dc.contributor.author | Grachev, Mikhail K. | |
| dc.contributor.author | Gorelik, Mikhail V. | |
| dc.date.accessioned | 2018-07-13T06:23:50Z | |
| dc.date.available | 2018-07-13T06:23:50Z | |
| dc.date.issued | 2014-04 | |
| dc.identifier.citation | Open Journal of Synthesis Theory and Applications, 2014, 3, 15-20 | en_US |
| dc.identifier.issn | 2168-1252 | |
| dc.identifier.uri | http://dx.doi.org/10.4236/ojsta.2014.32003 | |
| dc.identifier.uri | http://hdl.handle.net/123456789/1886 | |
| dc.description.abstract | Action of bromine in concentrated nitric acid allows carrying out mono- and polybromination of
moderately deactivated aromatic compounds. 4-Chloronitrobenzene and isophthalic acid turnes
into 3-bromo-4-chloronitrobenzene and 5-bromoisophthalic acid at reaction with bromine in
concentrated nitric acid at 20˚C whereas in absence of bromine in the same conditions 4-chloro-1,
3-dinitrobenzene and 5-nitroisophthalic acid are formed accordingly. Presence of bromine in
concentrated nitric acid changes nitrating capacity to brominating one. Terephthalic acid and
phthalic anhydride at heating with bromine in concentrated nitric acid can be transformed to appropriating
tetrabromo substituted compounds. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Scientific Research | en_US |
| dc.subject | Bromination | en_US |
| dc.subject | Nitration | en_US |
| dc.subject | Aromatic Compounds | en_US |
| dc.subject | 3-Bromo-4-chloronitrobenzene | en_US |
| dc.subject | 5-Bromoisophthalic Acid | en_US |
| dc.subject | 2,3,5,6-Tetrabromoterephthalic Acid | en_US |
| dc.subject | 3,4,5,6-Tetrabromophthalic Anhydride | en_US |
| dc.title | Aromatic Bromination in Concentrated Nitric Acid | en_US |
| dc.type | Article | en_US |
