One-pot methodology for conversion of o-halogen nitrobenzenes to benzofuroxans
Article
-
- Overview
-
- Research
-
- Identity
-
- Additional Document Info
-
- View All
-
Overview
abstract
-
Reaction of o-halonitrobenzenes with sodium azide under reflux of DMF/H2O gives benzofuroxans in one step in moderate to good yields. This is a faster methodology compared to the conventional procedure involving the preparation and subsequent pyrolysis of o-nitrophenyl azides. For comparison, the reaction was also performed under phase-transfer catalysis. © 2017 Taylor %26 Francis.
-
Reaction of o-halonitrobenzenes with sodium azide under reflux of DMF/H2O gives benzofuroxans in one step in moderate to good yields. This is a faster methodology compared to the conventional procedure involving the preparation and subsequent pyrolysis of o-nitrophenyl azides. For comparison, the reaction was also performed under phase-transfer catalysis. © 2017 Taylor & Francis.
publication date
published in
Research
keywords
-
Benzofuroxan; heterocycle; o-nitrophenyl azide; SNAr benzene derivative; dichloroethane; halogen; heterocyclic compound; nitrobenzene derivative; sodium azide; tetrylammonium; Article; cyclization; halogenation; infrared spectroscopy; methodology; nuclear magnetic resonance; one pot synthesis; proton nuclear magnetic resonance; pyrolysis; reaction time; substitution reaction; ultraviolet spectroscopy
Identity
Digital Object Identifier (DOI)
Additional Document Info
start page
end page
volume
issue