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A Convenient Dediazoniation of Arenediazonium Tetrafluoroborates: Triethylamine Effects on Competitive Ionic and Radical Dediazoniation
Authors:Koon Ha Park  Yoon Hwan Cho
Institution:Department of Chemistry , Chungnam National University , Taejon, Korea , 305-764
Abstract:Triethylamine was very efficient in the dediazoniation of arenediazonium salt. The major product depended on the comparative molar ratio (r) of triethylamine to benzenediazonium salt. When r<0.5, anisole (ionic product) was a major, while benzene (radical product) was a major when r>1.
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