PERFLUOROACYL THIOPHENS .I. BEHAVIOUR OF 2-THIENYL METALS WITH PERFLUOROALIPHATIC ACID DERIVATIVES

被引:5
作者
JONES, E
MOODIE, IM
机构
[1] Arthur D. Little Research Institute, Musselburgh, Midlothian
[2] Department of Organic Chemistry, The University, Groningen
来源
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC | 1968年 / 10期
关键词
D O I
10.1039/j39680001195
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reaction of 2-thienyl-lithium with perfluoroaliphatio acids and their NN-diethyl amides gives anomalous results; either a perfluoroacyl thiophen or a thiophen-carboxylic acid or carboxamide is obtained, depending on the size of the perfluoroalkyl group. Hexafluoro-1,3-di-(2-thenoyl)propane has been prepared from 2-thienyl-magnesium bromide and perfluoroglutaryl dichloride.
引用
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页码:1195 / &
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