FIELD: organic chemistry.
SUBSTANCE: invention relates to method for production of fluorinated ketone of general formula 5 . Claimed method includes reaction of compound of formula 3 , containing at least 30 wt.% of fluorine with fluorine in liquid phase, containing solvent selected from group comprising perfluoroalkane, perfluorinated ester, perfluorinated polyether, chlorofuorohydrocarbon, chlorofluoropolyether, perfluoroalkylamine, inert liquid, compound of formula 2 , compound of formula 6 to produce compound of formula 4 , followed by dissociation of ester bond in formula 4 in presence of KF, NaF or activated carbon without solvent. In formulae: RA represents, optionally containing ether-forming oxygen atom, wherein each of said groups contains C1-C10 carbon atoms; RAF represents C1-C10-perfluorenated RA group; RB represents alkyl optionally containing ether-forming oxygen atom, partially halogenated alkyl, optionally containing ether-forming oxygen atom, wherein each of said groups contains C1-C10 carbon atoms; RBF represents C1-C10-perfluorenated RB group; RC and RCF groups are identical ones and each RC and RCF contains C2-C10 carbon atoms and represents perfluorenated alkyl optionally containing ether-forming oxygen atom, partially halogenated alkyl, optionally containing ether-forming oxygen atom or RA and RB together form alkylene group optionally containing ether-forming oxygen atom, partially halogenated alkylene, optionally containing ether-forming oxygen atom, wherein each abovementioned group contains C3-C6 carbon atoms; each RAF and RBF are perflurenated RA and RB groups containing C3-C6 carbon atoms; groups are identical ones and each RC and RCF contains C2-C10 carbon atoms and represents perfluorenated alkyl optionally containing ether-forming oxygen atom, partially halogenated alkyl, optionally containing ether-forming oxygen atom. Method of present invention provides fluorinated ketone production with 71-96 % yield. Some intermediates of formula 3 also are described.
EFFECT: method for fluorinated ketone production with increased yield.
10 cl, 5 ex
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Authors
Dates
2006-07-10—Published
2001-08-30—Filed