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以β－苯乙胺和对硝基苯基溴乙基醚反应生成Ｎ－（对硝基苯氧乙基）β－苯乙胺和其重排产物Ｎ－（２－苯乙基）Ｎ－（２－羟乙基）－对硝基苯胺为例，研究分子内激活的亲核芳香取代反应——Ｎ－Ｏ型Ｓｍｉｌｅｓ重排的动力学过程。
The reaction of β-phenylethylamine and p-nitrophenyl ethyl bromide to form N- (p-nitrophenoxyethyl) β-phenylethylamine and its rearrangement product N- (2-phenylethyl) N- (2-hydroxyethyl) -p-nitroaniline was used as an example to study the kinetics of intramolecular aromatic nucleophilic substitution-N-O Smiles rearrangement.