Reinvestigation of the Reaction of Caro's Acid with 3-Aminopyrideine. An Improved Synthesis and Characterization of 3,3′-Azoxypyridine
作者:
AlbertE. Hauck,
C.S. Giam,
期刊:
Synthetic Communications
(Taylor Available online 1978)
卷期:
Volume 8,
issue 2
页码: 109-115
ISSN:0039-7911
年代: 1978
DOI:10.1080/00397917808062104
出版商: Taylor & Francis Group
数据来源: Taylor
摘要:
Pursuant to our interest in the effects of β-substituents upon the gas phase basicities of heteroaromatic compounds, we needed various mono-substituted pyridines, especially 3-nitropyridine. Reports concerning the synthesis of this compound include the direct electrophilic nitration of pyridine,1and the perhydrol oxidation of 3-aminopyridine.2,3The procedures for both methods were unattractive and the yields poor. Recently a convenient preparation of 3-nitropyridine via Caro's acid4oxidation of 3-aminopyridine was reported.5Although this report has been widely referenced, it did not provide experimental details, such as procedure, yields, or spectral characterization.
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