FIELD: organic chemistry. SUBSTANCE: products: amides and esters of perfluoropolyoxaalkylenesulfo- or perfluoropolyoxaalkylene carboxylic acids of the general formula where RFCF3O-, C2H5O-, C3F7O-;
; (_CF2CF2O)nCF2-,;
, n 8-5; Z=-CO-, -SO2-,; Q = -N(CmH2mOH)2, where m 2,3,4,6,8,10; -N[(C2H4O)4C3H6OH];; NHC2H4ORn, where Rn= CH3, C2H5, C3H7, -NH(C2H4O)5H, OCeH2eN(CeH2eOH) where e 2,4; CkH2k+1O, where R 6, 8, 10. Compound is synthesized by mixing fluoroanhydride of perfluoropolyoxaalkylenesulfo- or perfluoropolyoxaalkylene carboxylic acid of the general formula
where RF=CF3,
-(CF2CF2CF2O)nCF2CF2-,; n 8-55; Z -CO-, -SO2-, with primary, secondary or tertiary amine or alkanoylamine of the general formula H3-xN(R)x where X 1, 2, 3; R R=(CnH2nOH)x, where n 2, 3, 4, 6, 8, 10; -[(C2H4O)4C3H6OH]x at X 2 or -(C2H4OCH3)x,, -(C2H4OC2H5)x,, -(C2H4OC3H7)x,, -[(C2H4O)5-H]x at X 1 or (CnH2nOH)x,; X 3; n 2, 4, or higher fatty alcohol of the general formula CnH2n+1OH where n 6, 8, 10, and compound from the group: alkaline or alkaline-earth metal fluoride, ammonium fluoride or aluminium fluoride, alkaline metal carbonate, hydrocarbonate at molar ratio of indicated compounds 1.0: (1.2-4.0):(1.5-3.0), respectively, at (-25) (+8) C followed by heating up to 40-60 C, keeping reaction mixture at this temperature for 0.6-3.0 hr and isolation of the end product. Mixing parental products of reaction can be carried out in the presence of polyfluorocarbon solvent. Synthesized compounds were used for preparing antifriction, antiwearing, antiscratching addition agents to lubricant oils and as protective coating against atmosphere corrosion. EFFECT: improved method of synthesis, enhanced quality of products. 4 cl
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Authors
Dates
1995-10-10—Published
1994-02-04—Filed