22156-88-3Relevant academic research and scientific papers
DMD Oxidation of in-Situ-Generated σH Adducts Derived from Nitroarenes and the Carbanion of 2-Phenylpropionitrile to Phenols: The First Direct Substitution of a Nitro by a Hydroxy Group
Adam, Waldemar,Ma?kosza, Mieczyslaw,Staliński, Krzysztof,Zhao, Cong-Gui
, p. 4390 - 4391 (2007/10/03)
The dimethyldioxirane (DMD) oxidation of σH adducts derived from nitroarenes and the carbanion of 2-phenyIpropionitrile yields unexpectedly the phenols 5 as the major products, while the usually observed nitroarenes 4 are formed in very little
Oxidative nucleophilic substitution of hydrogen in nitroarenes
Makosza, Mieczyslaw,Stalinski, Krzysztof
, p. 2025 - 2031 (2007/10/03)
Carbanions of 2-phenylpropionitrile were found to add to nitroarenes in liquid ammonia to form σ(H) adducts, which were oxidized with KMnO4 to yield products of oxidative nucleophilic substitution of hydrogen (ONSH) in the position para to the nitro group. Treatment of the carbanion-nitroarene system with methyl iodide at -70°C indicated that the addition proceeds almost to completion. Thus, for the first time, the persistence of σ(H) adducts, formed between free anions and mononitroarenes, has been demonstrated. It was also shown that KMnO4, oxidizes σ(H) adducts to nitrobenzene faster than it does carbanions. This selective ONSH in the para positions of nitroarenes is a general process. However, some substituents hinder or inhibit the oxidation step.
