An environmentally benign synthesis of organic ammonium tribromides (OATB) and bromination of selected organic substrates by tetrabutylammonium tribromide (TBATB)
1998; Elsevier BV; Volume: 39; Issue: 44 Linguagem: Inglês
10.1016/s0040-4039(98)01818-8
ISSN1873-3581
AutoresMihir K. Chaudhuri, Abu T. Khan, Bhisma K. Patel, Deepa Dey, Wancydora Kharmawophlang, T. R. LAKSHMIPRABHA, Gagan C. Mandal,
Tópico(s)Oxidative Organic Chemistry Reactions
ResumoStable crystalline organic ammonium tribromides (OATB), like Me4NBr3, Et4NBr3, Bu4NBr3, cetyltrimethylammonium tribromide, PyHBr3, can be readily synthesised from the reaction of the corresponding bromides with V2O5 and aqueous H2O2. Typically, TBATB, Bu4NBr3, brominates a variety of organic substrates rather easily under mild conditions. An activated aromatic ring is selectively brominated in the presence of an olefinic double bond.
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