Journal of fluorine chemistry

On the electrochemical fluorination of aminoethers to give perfluoroaminoethers: possible candidates for blood substitutes

A Dimitrov, W Radeck, VE Platonov

Index: Dimitrov, A.; Radeck, W.; Ruediger, St.; Platonov, V.E. Journal of Fluorine Chemistry, 1991 , vol. 52, # 3 p. 317 - 331

Full Text: HTML

Citation Number: 14

Abstract

Abstract Aminoethers, ROC 2 H 4 NCH2CH2OCH2CH 2 (R= C 6 H 5, C 6 F 5, C 2 H 5), C 6 F 5 OC 2 H 4 N [CH 2] 5, were electrofluorinated in anhydrous hydrogen fluoride, the corresponding saturated perfluoroaminoethers being the largest individual substances in each case. One of them, F-[4-(2-cyclohexyloxyethyl) morpholine], has promising properties as a blood substitute.