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    • 91. 发明专利
    • Method for producing 2-trifluoromethyl-5-fluorobenzaldehyde and its derivative
    • 生产2-三氟甲基-5-氟代甲醛及其衍生物的方法
    • JP2006160635A
    • 2006-06-22
    • JP2004351728
    • 2004-12-03
    • Central Glass Co Ltdセントラル硝子株式会社
    • NISHINOMIYA TAKAYUKIFUKUI AKIHIRO
    • C07C45/43C07B61/00C07C29/141C07C33/46C07C47/55C07C51/235C07C51/58C07C63/70C07C209/40C07C211/29
    • PROBLEM TO BE SOLVED: To provide an advantageous method for producing 2-fluoromethyl-5-fluorobenzaldehyde and its derivative useful for intermediates of drugs and agricultural chemicals and the like on an industrial scale. SOLUTION: The method for producing 2-fluoromethyl-5-fluorobenzaldehyde comprises chlorinating 3,4-dimethylfluorobenzene with chlorine (Cl 2 ) to form an isomer mixture (a chlorinated reaction mixture) of 2-trichloromethyl-5-fluorobenzal chloride and 2-trichloromethyl-4-fluorobenzal chloride, bringing the obtained isomer mixture into contact with hydrogen fluoride (HF) to obtain a fluorinated reaction mixture, subjecting the fluorinated reaction mixture to distillation to efficiently isolate 2-fluoromethyl-5-fluorobenzal chloride, and hydrolyzing the obtained 2-fluoromethyl-5-fluorobenzal chloride to obtain 2-fluoromethyl-5-fluorobenzaldehyde. The 2-fluoromethyl-5-fluorobenzaldehyde can be thereafter converted into various derivatives. COPYRIGHT: (C)2006,JPO&NCIPI
    • 待解决的问题:为工业规模提供可用于药物和农药等中间体的2-氟甲基-5-氟苯甲醛及其衍生物的有利方法。 解决方案:2-氟甲基-5-氟苯甲醛的制备方法包括用氯(Cl 2 )氯化3,4-二甲基氟苯,以形成2-氟甲基-5-氟苯甲醛的异构体混合物(氯化反应混合物) 三氯甲基-5-氟苯甲酰氯和2-三氯甲基-4-氟亚苄基氯,使得到的异构体混合物与氟化氢(HF)接触,得到氟化反应混合物,使氟化反应混合物蒸馏,有效地分离出2-氟甲基 - 并将得到的2-氟甲基-5-氟苯甲醛水解,得到2-氟甲基-5-氟苯甲醛。 然后可以将2-氟甲基-5-氟苯甲醛转化成各种衍生物。 版权所有(C)2006,JPO&NCIPI
    • 96. 发明专利
    • JPH05339214A
    • 1993-12-21
    • JP14393992
    • 1992-06-04
    • MITSUI TOATSU CHEMICALS
    • KAMEOKA TAIJITAKAGI MASATOSHIKATO TOSHIOHASEYAMA RYUJI
    • C07C209/40C07C211/49
    • PURPOSE:To produce the subject compound in a high yield and in a high purity by catalytically reducing nitroacetophenone oxime readily producible from nitroacetophenone as a raw material in the presence of a reducing catalyst under CO2. CONSTITUTION:Nitroacetophenone oxime of formula I (nitro group is o-position, m-position or p-position) is catalytically reduced in the presence of carbon dioxide in an organic solvent to obtain alpha-(aminophenyl)ethylamine of formula II. In the reaction the product can be obtained as the carbonate salt of alpha-(aminophenyl)ethylamine in a stable form, because the carbon dioxide turns into carbonic acid in the presence of water. Various intermediates such as amines or imines produced in the reduction reaction are stabilized as carbonate salts only by introducing the carbon dioxide into the reaction system, whereby the decompositions of the products and side reactions are suppressed. alpha-(Aminophenyl)ethylamine is useful as a curing agent for epoxy resins, polyurethane resins or polyurea resins, as a raw material for polyamides or polyimides, etc.