REACTIONS INVOLVING FLUORIDE-ION .39. REACTIONS OF PERFLUORINATED DIENES WITH OXYGEN AND SULFUR NUCLEOPHILES

被引:23
作者
BRISCOE, MW [1 ]
CHAMBERS, RD [1 ]
MULLINS, SJ [1 ]
NAKAMURA, T [1 ]
VAUGHAN, JFS [1 ]
机构
[1] UNIV DURHAM,DEPT CHEM,SCI LABS,DURHAM DH1 3LE,ENGLAND
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1994年 / 21期
关键词
D O I
10.1039/p19940003119
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The order of reactivity of perfluorinated dienes towards methanol is 3 > 2 much greater than 1 and the process is activated by release of angle strain. The diene 1 is hydrolysed to give perfluorotetramethyl-furan and the corresponding thiophene, is obtained by an analogous process using K2S. Hydrolysis of compounds 2 and 3 yields diketones that are strong acids. Reactions of phenols and thiophenols with 1 give aryl ethers and sulfides and difunctional nucleophiles react with 1 to give potential polymer precursors.
引用
收藏
页码:3119 / 3124
页数:6
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