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    • 45. 发明授权
    • Process for the preparation of trifluoromethyl containing derivatives
    • 制备含三氟甲基衍生物的方法
    • US6111130A
    • 2000-08-29
    • US307819
    • 1999-05-10
    • Michael Van Der Puy
    • Michael Van Der Puy
    • C07C17/25C07C17/358C07C29/09C07C29/17C07C67/11C07C69/76
    • C07C17/358C07C17/25C07C29/095C07C29/172C07C67/11
    • The present invention relates to a process for the preparation of trifluoromethylated derivatives of the formula CF.sub.3 CCl.dbd.CHCH.sub.2 OC(.dbd.O)R, wherein R is unsubstituted or substituted C.sub.1 to C.sub.6 straight chain or branched alkyl, unsubstituted or substituted C.sub.3 to C.sub.7 cycloalkyl, unsubstituted or substituted C.sub.2 to C.sub.12 alkenyl, a benzyl group unsubstituted or substituted with R', a phenyl group unsubstituted or substituted with R'; R' is an unsubstituted or substituted C.sub.1 to C.sub.6 straight chain or branched alkyl; and wherein where R and/or R' are substituted each is substituted with R', by reaction of HCFC-353 with carboxylic acid salts. The trifluoromethylated derivatives, particularly CF.sub.3 CCl.dbd.CHCH.sub.2 OC(.dbd.O)CH.sub.3, are versatile intermediates for the synthesis of a wide variety of trifluoromethylated organic compounds, which find utility as pharmaceuticals, agricultural chemicals, and materials such as liquid crystals.
    • 本发明涉及制备式CF 3 CCl = CHCH 2 OC(= O)R 3的三氟甲基化衍生物的方法,其中R是未取代或取代的C1至C6直链或支链烷基,未取代或取代的C3至C7环烷基,未取代或未取代的 取代的C2至C12烯基,未取代或被R'取代的苄基,未取代或被R'取代的苯基; R'是未取代或取代的C1至C6直链或支链烷基; 并且其中当R和/或R'被取代时,通过HCFC-353与羧酸盐的反应被R'取代。 三氟甲基化衍生物,特别是CF 3 CCl = CHCH 2 OC(= O)CH 3,是用于合成各种三氟甲基化有机化合物的通用中间体,其可用作药物,农药和诸如液晶的材料。