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AMIDES AND ETHERS OF PERFLUOROPOLYOXYALKYLENE SULPHONIC- OR PERFLUOROPOLYOXYALKYLENE CARBOXYLIC ACIDS AND A METHOD OF OBTAINING THE SAME
AMIDES AND ETHERS OF PERFLUOROPOLYOXYALKYLENE SULPHONIC- OR PERFLUOROPOLYOXYALKYLENE CARBOXYLIC ACIDS AND A METHOD OF OBTAINING THE SAME
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机译:全氟聚氧亚烷基磺基或全氟聚氧亚烷基羧酸的酰胺和醚及其获得方法
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摘要
Amides and ethers of perfluoropolyoxyalkylene sulphonic- or perfluoropolyoxyalkylene carboxylic acids of general formula (I): RFR¹FZQ wherein: RF represents CF₃O-, C₂F₅O-, C₃F₇O-, C₈F₁₇O-, R¹F represents (a), -(CF₂CF₂O)nCF₂, - (CF₂CF₂CF₂O)nCF₂CF₂-, n being 8-55; Z represents -CO-, -SO₂-; Q represents -N(CmH2mOH)₂, where m = 2, 3, 4, 6, 8, 10, - N((C₂H₄O)₄C₃H₆OH)₂, -NHC₂H₄ORn, where Rn = CH₃, C₂H₅, C₃h₇, -NH(C₂H₄O)₅H, OCLH2LN(CLH2LOH)₂, where L = 2,4 CKH2K+1O-, where k = 6, 8, 10. The proposed method of obtaining compounds of general formula (I) involves mixing an anhydrous fluoride of general formula RFR¹FZF, in which RF, R¹F, n and Z have the meanings shown above, with a secondary or tertiary amine or alkanolamine of general formula H3-XN(R)X, in which x = 1, 2, 3 and R represents: - (CnH2nH)x where n = 2, 3, 4, 6, 8, 10; -((C₂H₄O)₄C₃H₆OH)X where x = 2 or 1; -(C₂H₄OCH₃)₃, -(C₂H₄OC₂H₅)X, - (C₂H₄OC₃H₇)X, or -((C₂H₄O)₅H)X where x = 1; or(CnH2nOH)x where x = 3 and n = 2 or 4, at a temperature of between -25 and +8 oC; or alternatively with a higher fatty alcohol CnH2n+1OH, where n = 6, 8, 10, and with a compound chosen from the following: an alkali metal- or alkaline-earth metal fluoride, ammonium or aluminium fluoride, and alkali metal carbonate or bicarbonate. The molar ratios of these compounds are 1; (1.2 - 4): 1.5: 3, as appropriate. The mixture is subsequently heated to 40-60 oC and allowed to stand at that temperature for 0.6-3.0 hours before the target product is removed.
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机译:通式(I)的全氟聚氧化烯磺酸或全氟聚氧化烯羧酸的酰胺和醚:R F Sub>R¹ F Sub> ZQ其中:R F Sub>代表CF representsO -,C 2 F 3 O-,C 3 F 3 O-,C 3 F 6 O-,R 1 F表示[a],-(CF 2 CF 2 O)n CF>,-(CF 2 CF 2 CF 2 O) Sub > CF 2 CF 2-,n为8-55; Z代表-CO-,-SO 2-; Q代表-N(C m Sub> H 2m Sub> OH)2,其中m = 2、3、4、6、8、10,-N((C 2H₄O)₄C₃H₆OH) 1,2,-NHC 2H₄OR n Sub>,其中R n Sub> = CH 3,C 2 H 3,C₃h₇,-NH(C 2 H 3 O)₅H,OC L Sub> H 2L Sub> N(C L Sub> H 2L Sub> OH)2,其中L = 2,4 C K Sub> H 2K + 1 Sub> O-,其中k = 6、8、10。拟议的获得通式(I)化合物的方法包括将通式R F Sub>R¹的无水氟化物混合F Sub> ZF,其中R F Sub>,R¹ F Sub>,n和Z具有以上所示的含义,且具有通式H的仲或叔胺或链烷醇胺 3-X Sub> N(R) X Sub>,其中x = 1,2,3和R表示:-(C n Sub> H 2n Sub> H) x Sub>其中n = 2、3、4、6、8、10; -((C 2H₄O)₄C₃H₆OH) X Sub>其中x = 2或1; -(C 2H₄OCH3)₃,-(C 2H₄OC2H₅) X Sub>,-(C 2H₄OC₃H₇) X Sub>或-((C 2H₄O)₅H) X Sub> = 1;或(C n Sub> H 2n Sub> OH) x Sub>其中x = 3且n = 2或4,在-25至+ 8 o Sup> C;或者使用高级脂肪醇C n Sub> H 2n + 1 Sub> OH,其中n = 6、8、10,以及选自以下的化合物:碱金属-或碱土金属氟化物,铵或铝氟化物,以及碱金属碳酸盐或碳酸氢盐。这些化合物的摩尔比为1。 (1.2-4):1.5:3,视情况而定。随后将混合物加热至40-60℃,并在该温度下静置0.6-3.0小时,然后除去目标产物。
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