684-23-1Relevant academic research and scientific papers
Polyfluorinated Organic Compounds. X. Reaction of Perfluoro(2-methyl-2-pentene) with Sodium Azide
Zhuzhgov,Furin
, p. 710 - 714 (2007/10/03)
Perfluoro(2-methyl-2-pentene) reacts with sodium azide in acetonitrile at -10°C to yield perluoro-(3-azido-2-methyl-2-pentene), which is stable only at low temperature. When the reaction is carried out in the presence of ethanol at the same temperature, stable 5-ethoxy-5-pentafluoroethyl-4,4-bis(trifluorornemyl)-4,5-dihydro-1H-1,2,3- triazole is formed. The reaction in the system acetonitrile-ethanol at 2°C yields ethyl pentafluoropropanimidate and bis(trifluoromethyl)diazomethane. Thermolysis and photolysis of perfluoro-(3-azido-2-methyl-2-pentene) in CCl4, as well as in C6H6, toluene, or pentane, results in fromation of 3-pentafluoroethyl-2,2-bis(trifluoromethyl)-2H-azirine.
PERFLUOROALKYL DERIVATIVES OF NITROGEN. PART LIII. REACTION OF PERFLUORO(2,5-DIMETHYL-4-OXA-3,5-DIAZAHEX-2-ENE) WITH FLUORO-OLEFINS
Fisher, R.,Haszeldine, R. N.,Tipping, A. E.
, p. 155 - 164 (2007/10/02)
Thermal decomposition of the title compound at 140 deg C gives mainly nitrogen, hexafluoroacetone and tetrakistrifluoromethylhydrazine while reaction with tetrafluoroethylene and chlorotrifluoroethylene affords equimolar mixtures of the 1:1 adducts (CF3)2C=NCF2CFXON(CF3)2 and (CF3)2C=NOCFXCF2N(CF3)2 (X=F and Cl) in highly yield via four-centre addition or a radical-cage process.
