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    • 5. 发明授权
    • Selective chlorination of chlorotrifluoroethylene telomers
    • 选择性氯化氯三氟乙烯调聚物
    • US4801763A
    • 1989-01-31
    • US78327
    • 1987-07-27
    • James J. MaulBobby F. DannelsDavid Y. Tang
    • James J. MaulBobby F. DannelsDavid Y. Tang
    • C07C17/395C07C17/20C07C17/38C07C19/08C07G13/00
    • C07C17/395
    • A process is disclosed for purifying and stabilizing a mixture of regular chlorotrifluoroethyelne telomers of formula RCXCl(CF.sub.2 CFCl).sub.n Br from bromine-containing irregular telomer impurities of similar molecular weight. The telomer mixture is produced by reacting chlorotrifluoroethylene with a telogen of formula RCXClBr, where R is CF.sub.2 Br, or Cl, and X is Cl or F. The telomer mixture is then chlorinated using either elevated temperature alone (100.degree. C.-350.degree. C.), or a combination of elevated temperatures (100.degree. C.-200.degree. C.) and light energy primarily of the wavelength region greater than about 3000.degree.A. Under these conditions, CFClBr telomer end group of the regular or normal telomer is chlorinated to form --CFCl.sub.2 end groups, while the bromine-containing irregular telomer impurities (whose bromine-containing end groups are substantially only --CF.sub.2 Br) are substantially not chlorinated. The desired regular telomers can then be readily separated from the higher boiling impurities by distillation. Any --CF.sub.2 Br groups present in the isolated regular telomer are then further stabilized by prolonged chlorination under the above conditions or at elevated temperatures (100.degree. C.-350.degree. C.) with irradiation by a UV lamp.
    • 公开了一种用于纯化和稳定式RCXCl(CF 2 CFCl)nBr的常规氯三氟乙烯调节剂的混合物的方法,该混合物含有相似分子量的含溴不规则调聚物杂质。 调聚物混合物通过使氯三氟乙烯与式RCXClBr的脱水酶(其中R是CF 2 Br或Cl,X是Cl或F)反应来制备。然后使用单独的升高温度(100℃-350℃)将调聚物混合物进行氯化 )或高温(100℃-2200℃)和主要波长区域的光能大于约3000°A的组合。在这些条件下,常规或正常调聚物的CFClBr调聚端基是 氯化形成-CFCl 2端基,而含溴不规则调聚剂杂质(其含溴端基本上仅为-CF 2 Br)基本上不氯化。 然后可以通过蒸馏将所需的常规调聚物容易地与较高沸点的杂质分离。 然后通过在上述条件下或在升高的温度(100℃-350℃)下用UV灯照射,通过长时间氯化来进一步稳定分离的常规调聚物中存在的任何-CF 2 Br基团。
    • 10. 发明授权
    • Fluorinated carbocylic compounds
    • 氟化碳环化合物
    • US4792618A
    • 1988-12-20
    • US680695
    • 1984-12-12
    • Joseph F. BieronDavid Y. Tang
    • Joseph F. BieronDavid Y. Tang
    • C07C51/567C07C69/75C07C49/303C07C53/44C07C121/46
    • C07C51/567
    • Fluoro-substituted carbocyclic compounds are prepared by(A) reacting hydrogen fluoride with a chloro-cyclohexenyl compound of the formula ##STR1## where R.sub.1 and R.sub.2 are independently selected from the group consisting of --H, --CH.sub.2 OH, --COF, --COCl, --CF.sub.3, --CN, ##STR2## and --CH.sub.2 R, where R is --H or alkyl of 1-4 carbon atoms, to form a gem-dihalocyclohexane compound of the formula ##STR3## where X is chlorine and R.sub.1 and R.sub.2 are as defined above, (B) dehydrohalogenating the gem-dihalocyclohexane compound in the vapor phase to form a fluoro-cyclohexenyl compound of the formula ##STR4## (C) contacting the fluoro-cyclohexenyl compound, in the vapor phase, with a dehydrogenation catalyst to form a fluoro-substituted aromatic compound of the formula ##STR5##
    • 氟取代的碳环化合物是通过(A)使氟化氢与式(IMAGE)的氯 - 环己烯基化合物反应来制备的,其中R 1和R 2独立地选自-H,-CH 2 OH,-COF,-COCl, -CF 3,-CN,和-CH 2 R,其中R是-H或1-4个碳原子的烷基,以形成式为“IMAGE”的偕 - 二卤代环己烷化合物,其中X为氯,R 1和R 2为 (B)在蒸气相中脱氢卤化偕 - 二卤代环己烷化合物以形成下式的氟 - 环己烯基化合物:(C)使气相中的氟 - 环己烯基化合物与脱氢催化剂接触形成 具有下式的氟取代的芳族化合物