667-49-2Relevant articles and documents
ELECTROPHILIC ALKENYLATION OF FLUOROOLEFINS BY PERFLUORO(2-ALKOXYPROPENES)
Chepik, S. D.,Belen'kii, G. G.,German, L. S.
, p. 1712 - 1714 (1991)
Perfluoro(2-alkoxypropenes) react with tetrafluoroethylene under mild conditions in the presence of SbF5 to give the corresponding perfluoro(2-alkoxy-2-pentenes). 1-Trifluoromethoxyperfluoropropene is converted by the action of SbF5 in SO2ClF solution to the acid fluoride derivative of perfluoroacrylic acid.
Novel synthetic route to perfluoroallyl cyanide (PFACN) reacting perfluoroallyl fluorosulfonate with cyanide
Tverdomed, Sergey N.,Hirschberg, Markus E.,Pajkert, Romana,Hintzer, Klaus,R?schenthaler, Gerd-Volker
, p. 65 - 69 (2018/03/21)
A novel synthetic method for the preparation of perfluoroallyl cyanide CF2[dbnd]CFCF2CN (PFACN) is presented. This includes the addition – elimination reaction of cyanide anion with perfluoroallyl fluorosulfate CF2[dbnd]CF
EINSTUFIGE HERSTELLUNG HALOGENIERTER CARBONSAUREFLUORIDE AUS DEN FREIEN SAUREN
Schwertfeger, W.,Siegemund, G.
, p. 237 - 246 (2007/10/02)
The reaction of per- or polyhalogenated carboxylic acids with trifluoromethyl or difluorochloromethyl substituted aromatics takes place in the presence of Lewis-acid-catalysts and forms the corresponding acid fluorides in good to very good yields.