UNSYMMETRICALLY DISUBSTITUTED FERROCENES .4. SYNTHESIS AND REACTIVITY OF 2-(NN-DIMETHYLAMINOMETHYL)FERROCENEBORNONIC ACID

被引:47
作者
MARR, G
MOORE, RE
ROCKETT, BW
机构
[1] Department of Applied Science, Wolverhampton College of Technology, Wolverhampton
来源
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC | 1968年 / 01期
关键词
D O I
10.1039/j39680000024
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reaction of lithiated (NN-dimethylaminomethyl)ferrocene with tri-n-butyl borate has given [2-(NN-dimethylaminomethyl)ferroceneboronic acid. This amino-acid has been converted into the corresponding 2-chloro-, 2-bromo-, and 2-iodo-(dimethylaminomethyl)ferrocenes. The methiodides of these halo-amines underwent nucleophilic displacement reactions with amines, phenol, and aqueous sodium hydroxide to afford a variety of 2-halo-ferrocenes.
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页码:24 / &
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