74415-71-7Relevant academic research and scientific papers
Valence-bond isomer chemistry. Part 13. Photochemical oxidation of hexafluorobenzene: formation of hexafluoro-3-oxatricyclo2,4>hept-6-ene and its reactions
Barlow, Michael G.,Peck, Colin J.
, p. 179 - 192 (2007/10/02)
Vapour-phase ultraviolet irradiation of hexafluorobenzene in the presence of oxygen slowly yields hexafluoro-3-oxatricyclo2,4>hept-6-ene (2) (10percent).The CF=CF bond in 2 adds (yields of adducts given) the dienes; cyclopentadiene (74percent), furan (61percent) and 2,5-diphenylisobenzofuran (59percent); benzonitrile oxide (58percent); chlorine (59percent) and bromine (71percent) photochemically.Heptene 2 isomerises thermally hexafluorocyclohexa-2,4-dienone (6) (60percent) at 50 deg C, and reacts with diethyl ether at room temperature yielding ethyl fluoride (89percent) and 2-ethoxypentafluorocyclohexa-2,5-dienone (21percent).The benzonitrile oxide adduct, upon flow pyrolysis at 440 deg C, yields an isomeric oxepin derivative and the cyclohexadienone 6 with longer contact times.The chlorine adduct similarly yields a dichloro-oxepin derivative; attempts to dechlorinate this to hexafluoro-oxepin were unsuccessful.Benzonitrile oxide adds to one or both of the C=C bonds of hexafluorobicyclohexa-2,5-diene; the 1:1 adduct isomerises thermally to the benzonitrile oxide-hexafluorobenzene adduct.
Hexafluoro-3-oxatricyclo2,4>hept-6-ene (Hexafluoro-Dewar-benzene Oxide) from the Photochemical Oxidation of Hexafluorobenzene
Barlow, Michael G.,Haszeldine, Robert N.,Peck, Colin J.
, p. 158 - 159 (2007/10/02)
Photochemical oxidation of hexafluorobenzene in the vapour phase yields the title compound, which undergoes thermal rearrangement into hexafluorocyclohexa-2,4-dienone and two acid fluorides, attack by diethyl ether at the oxiran ring, and cycloaddition to its C=C double bond.
