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Regioselective bromination of aromatic amines and phenols using N-benzyl-DABCO tribromide

Matloubi Moghaddam, F ; Sharif University of Technology | 2009

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  1. Type of Document: Article
  2. DOI: 10.1080/00397910902898569
  3. Publisher: 2009
  4. Abstract:
  5. N-Benzyl-DABCO tribromide, a stable, solid organic ammonium tribromide, has been used as a bromine source for the regioselective and high-yielding bromination of aromatic amines and phenols. Mono-bromination proceeds well in the presence of a stoichiometric amount of bromine source at room temperature
  6. Keywords:
  7. Bromination ; Mono-bromoarenes ; N-benzyl-DABCO tribromide ; Organic ammonium tribromides ; 1 Bromo 2 naphthol ; 2 Bromo 4 nitroaniline ; 4 Bromophenol ; Aromatic amine ; Bromine derivative ; N,N dimethyl 4 bromoaniline ; Phenol derivative ; Unclassified drug ; Article ; Chemical structure ; Reaction time ; Room temperature
  8. Source: Synthetic Communications ; Volume 39, Issue 23 , 29 October , 2009 , Pages 4212-4220 ; 00397911 (ISSN)
  9. URL: https://www.tandfonline.com/doi/abs/10.1080/00397910902898569?scroll=top&needAccess=true&journalCode=lsyc20