On the synthesis of 2-amino-4,6-difluorobenzonitrile: Highly selective formation of 5-fluoro-3-nitro-1,2-benzoquinone 2-diazide in the attempted Sandmeyer cyanation of 2,4-difluoro-6-nitrobenzenediazonium cation

被引:3
作者
Camps, P [1 ]
Morral, J [1 ]
Munoz-Torrero, D [1 ]
机构
[1] Univ Barcelona, Fac Farm, Quim Farmaceut Lab, E-08028 Barcelona, Spain
关键词
D O I
10.1039/a707205h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Attempted cyanation of a diazonium salt derived from 2,4-difluoro-6-nitroaniline gives 5-fluoro-3-nitro-1,2-benzoquinone 2-diazide double dagger in good yield by selective nucleophilic substitution of the 2-fluoride group by hydroxide, instead of the desired 2-amino-4,6-difluorobenzonitrile, which can be obtained by the reaction of 2,4,6-trifluorobenzonitrile with ammonia.
引用
收藏
页码:144 / 145
页数:3
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