A convenient dediazoniation of arenediazonium tetrafluoroborates: Triethylamine effects on competitive ionic and radical dediazoniation

Article abstract of DOI:10.1080/00397919608003524

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.

Full text of DOI:10.1080/00397919608003524

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Convenient Dediazoniation
of Arenediazonium
Tetrafluoroborates:
Triethylamine Effects on
Competitive Ionic and Radical
Dediazoniation
Koon Ha Park a & Yoon Hwan Cho a
a Department of Chemistry, Chungnam National
University, Taejon, Korea, 305-764
Version of record first published: 15 Aug 2006.
To cite this article: Koon Ha Park & Yoon Hwan Cho (1996): A Convenient
Dediazoniation of Arenediazonium Tetrafluoroborates: Triethylamine Effects on
Competitive Ionic and Radical Dediazoniation, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 26:8,
1569-1574
To link to this article: http://dx.doi.org/10.1080/00397919608003524
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