The electrochemical fluorination of nitrogen-containing carboxylic acids. Fluorination of dimethylamino- or diethylamino-substituted carboxylic acid derivatives
The electrochemical fluorination of six derivatives of dimethylamino- or diethylamino-substituted carboxylicacids has been conducted. As the main fluorination products, cyclized and cleaved products as well as the desired N-containing perfluoroacid fluorides were formed, and their ratios depended on the chain length and the structure of the starting carboxylicacids, and the nature of the dialkylamino
The electrochemical fluorination of N-containing carboxylic acids (Part 4). Fluorination of methyl 3-dialkylamino-isobutyrates and methyl 3-dialkylamino-n-butyrates
作者:Takashi Abe、Haruhiko Fukaya、Eiji Hayashi、Yoshio Hayakawa、Masakazu Nishida、Hajime Baba
DOI:10.1016/0022-1139(93)03019-i
日期:1994.2
Several methylesters of 3-dialkylamino-substituted n- and isobutyric acids have been subjected to electrochemical fluorination to give the corresponding perfluoroacid fluorides. Dimethyl, diethyl, pyrrolidino, morpholino, piperidino and N-methylpiperazino groups were investigated as dialkylamino substituents. The structure/yield relationship was evaluated both in terms of the structure of the acid and
Described herein is fluorinated dye comprising: a fluorescing coumarin-derived moiety connected to an oligomer of hexafluoropropylene oxide via a non-fluorinated divalent linking group. Such fluorinated dyes are soluble in fluorinated fluids and may be used to detect leaks in various systems such as refrigerant, air conditioning and/or heat transfer systems.
Six methyl esters of 3-dialkylamino-substituted propionic acids were subjected to electrochemicalfluorination to give the corresponding perfluoroacid fluorides. The following dialkylamino substituents were investigated: diethylamino, di-n-propyl-amino, di-n-butylamino, pyrrolidino, morpholino and piperidino groups. These perfluoroacid fluorides, which were obtained in fair yields, are considered to
将3-二烷基氨基取代的丙酸的六种甲酯进行电化学氟化,得到相应的全氟代氟化物。研究了以下二烷基氨基取代基:二乙基氨基,二正丙基氨基,二正丁基氨基,吡咯烷基,吗啉代和哌啶子基。这些以合理收率获得的全氟酸氟化物被认为是制备软质(可降解)含氟化合物的潜在关键前体。这些盐在水溶液中显示出明显降低的表面张力。报告了所获得的所有全氟酸氟化物的物理性质,以及它们的光谱数据(19 F NMR,质谱和IR光谱)。
The electrochemical fluorination of nitrogen-containing carboxylic acids. Fluorination of methyl esters of cyclic amino-group substituted carboxylic acids
作者:Takashi Abe、Eiji Hayashi、Haruhiko Fukaya、Hajime Baba
DOI:10.1016/s0022-1139(00)80494-7
日期:1990.11
Nine methyl esters of cyclic amino-group substituted carboxylic acids related to glycine, alanine or β-alanine were subjected to electrochemicalfluorination. This afforded the corresponding perfluoroacid fluorides together with cleavage products in fair yields. As cyclic amino-substituents, pyrrolidino-, morpholino-, piperidino-, hexamethyleneimino- and N′-methyl-piperazinyl-groups were investigated
对与甘氨酸,丙氨酸或β-丙氨酸有关的环状氨基取代的羧酸的九种甲酯进行电化学氟化。这样以合理的产率得到了相应的全氟氟化物和裂解产物。作为环状氨基取代基,研究了吡咯烷基,吗啉代,哌啶子基,六亚甲基亚氨基和N'-甲基哌嗪基。未观察到环化副产物的形成,这与脂族二烷基氨基取代的羧酸的氟化形成对比。从这样的2-环氨基丙酸甲酯[环氨基:吡咯烷基,吗啉代或哌啶子基],与全氟酸氟化物一起得到全氟甲基酯,产率为1-2%和14-29。 % 分别。前一种化合物的形成归因于庞大的环状氨基的阻断作用。报告了所获得的新化合物的物理性质及其光谱(19 F NMR,质量和IR)数据。