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    • 1. 发明专利
    • Method of producing difluoroacetic acid ester
    • 生产二油酸酯的方法
    • JP2013147474A
    • 2013-08-01
    • JP2012010822
    • 2012-01-23
    • Daikin Industries Ltdダイキン工業株式会社
    • ASADA DAISUKEOTSUKA TATSUYA
    • C07C67/00C07B61/00C07C69/63
    • PROBLEM TO BE SOLVED: To provide a method of producing a difluoroacetic acid ester with high selectivity in good yield while preventing generation of byproducts.SOLUTION: In a method of producing a difluoroacetic acid ester represented by general formula HCFCOOR wherein R is a lower alkyl group, 1,1,2,2-tetrafluoroethyl alkyl ether represented by general formula HCFCFOR wherein R is a lower alkyl group is brought into contact with an acid catalyst in the presence of an oxide and a lower alcohol represented by general formula ROH wherein R is a lower alkyl group. In the method, a reaction temperature is 20-60°C, and a usage amount of the acid catalyst is 0.1-0.5 mole for 1 mol of 1,1,2,2-tetrafluoroethyl alkyl ether.
    • 要解决的问题:提供以良好的产率以高选择性生产二氟乙酸酯的方法,同时防止产生副产物。方法:在制备由通式HCFCOOR表示的二氟乙酸酯的方法中,其中R是低级烷基 ,在通式ROH表示的氧化物和低级醇的存在下,通式为HCFCFOR的其中R为低级烷基的1,1,2,2-四氟乙基烷基醚与酸催化剂接触,其中R为 低级烷基。 在该方法中,反应温度为20-60℃,对于1摩尔1,1,2,2-四氟乙基烷基醚,酸催化剂的使用量为0.1-0.5摩尔。
    • 4. 发明专利
    • Method for producing fluoroalkyl ether
    • 生产氟烷基醚的方法
    • JP2011116661A
    • 2011-06-16
    • JP2008073082
    • 2008-03-21
    • Daikin Industries Ltdダイキン工業株式会社
    • SUGIYAMA AKIHIRASUZUKI ATSUSHIYAMAMOTO SADAHIROKUROKI YOSHICHIKAOTSUKA TATSUYA
    • C07C41/18C07C43/12
    • C07C41/18C07C43/12C07C43/123
    • PROBLEM TO BE SOLVED: To provide a method for easily producing a fluoroalkyl ether such as hexafluoroisopropylmethyl ether with high selectivity using an inexpensive raw material. SOLUTION: The method for producing a fluoroalkyl ether represented by formula (2) includes decarboxylating a compound represented by formula (1) in the presence of an amine compound and a hydrohalic acid. In the formulae, Rf 1 and Rf 2 may be the same or different and each represents a group: CF 3 (CF 2 ) n (wherein n is a natural number of 0 to 10) or a group: CH 3 (CH 2 ) m (wherein, m is a natural number of 0 to 10), provided that at least one of Rf 1 and Rf 2 represents the group: CF 3 (CF 2 ) n ; R 1 represents an alkyl group that may contain a substituent, an aryl group that may contain a substituent, or an alkenyl group that may contain a substituent; and X represents a hydrogen atom or a halogen atom. COPYRIGHT: (C)2011,JPO&INPIT
    • 要解决的问题:提供一种使用廉价的原料以高选择性容易地制备氟烷基醚如六氟异丙基甲基醚的方法。 解决方案:由式(2)表示的氟烷基醚的制备方法包括在胺化合物和氢卤酸的存在下使由式(1)表示的化合物脱羧。 在式中,Rf 1 和Rf 2 可以相同或不同,并且各自表示基团:CF 3 (其中n为0至10的自然数)或基团:CH 3 SB 3(CH 2 SB 2) SB> m (其中,m为0至10的自然数),条件是Rf 1 和Rf 2 中的至少一个表示基团: CF 3 (CF 2 名词; R 1表示可以含有取代基的烷基,可以含有取代基的芳基或可以含有取代基的烯基; X表示氢原子或卤素原子。 版权所有(C)2011,JPO&INPIT
    • 6. 发明专利
    • New carboxylic acid ester, application of the same and method for producing the same
    • 新型羧酸酯,其应用及其生产方法
    • JP2009120506A
    • 2009-06-04
    • JP2007294050
    • 2007-11-13
    • Daikin Ind Ltdダイキン工業株式会社
    • YAMAMOTO SADAHIROOTSUKA TATSUYA
    • C07C69/708C07C41/18C07C41/22C07C43/12C07C67/307
    • C07C69/708C07C41/18C07C67/307C07C43/123
    • PROBLEM TO BE SOLVED: To provide a method for producing 1,1,1,3,3,3-hexafluoroisopropyl fluoromethyl ether (sevoflurane) known as a compound having an anesthetic property, efficiently and inexpensively, and a new compound useful for producing the same. SOLUTION: This method for producing an α-chloromethoxy carboxylic acid ester expressed by general formula (1): (CF 3 ) 2 C(OCH 2 Cl)COOR [wherein, R is a hydrocarbon group which may have at least one of an atom selected from the group consisting of a halogen atom, O, N and S] is provided by reacting an α-methoxy carboxylic acid ester expressed by general formula (2): (CF 3 ) 2 C(OCH 3 )COOR [wherein, R is the same as above] with molecular chlorine, and the method for producing the 1,1,1,3,3,3-hexafluoroisopropyl fluoromethyl ether expressed by the chemical formula of (CF 3 ) 2 CH(OCH 2 F) is provided by fluorinating and de-carboxylating the α-chloromethoxy carboxylic acid ester. COPYRIGHT: (C)2009,JPO&INPIT
    • 待解决的问题:提供一种有效且廉价地制备具有麻醉性质的化合物1,1,1,3,3,3-六氟异丙基氟甲基醚(七氟烷)的方法,以及可用的新化合物 为了生产相同。 < P>解决方案:通式(1)表示的α-氯甲氧基羧酸酯的制造方法:(CF 3 SB 3)SB 其中R是可以具有选自卤素原子,O,N和S中的至少一个原子的烃基,其通过使α-甲氧基羧酸 由通式(2)表示的酯:(CF 3 SB 3)SB(CO 3)COOR [其中,R与上述相同 ]和由化学式(CF 3 2
    • 8. 发明专利
    • METHOD FOR PURIFYING FLUORO-β-DICARBONYL COMPOUND
    • JP2004307355A
    • 2004-11-04
    • JP2003099219
    • 2003-04-02
    • Daikin Ind Ltdダイキン工業株式会社
    • KARUBE DAISUKEOTSUKA TATSUYA
    • C07C67/60C07C67/307C07C67/54C07C69/716
    • PROBLEM TO BE SOLVED: To provide a method for purification by which a high-purity objective substance can efficiently be obtained from a fluoro-β-dicarbonyl compound containing a by-product such as a difluoro derivative without emitting an acidic gas, or the like, by decomposition.
      SOLUTION: This method for purifying a fluoro-β-dicarbonyl compound is characterized as follows. A mixture containing the fluoro-β-dicarbonyl compound represented by the formula (1) R
      1 COC R
      2 FCOR
      3 (wherein, R
      1 is hydrogen atom, a substituted or an unsubstituted alkyl group or a substituted or an unsubstituted aryl group; R
      2 is hydrogen atom, a halogen atom, a substituted or an unsubstituted alkyl group or a substituted or an unsubstituted aryl group; R
      3 is hydrogen atom, a substituted or an unsubstituted alkyl group, a substituted or an unsubstituted aryl group, a substituted or an unsubstituted alkoxy group or a substituted or an unsubstituted aryloxy group; or at least two of R
      1 , R
      2 and R
      3 together may form a part of a cyclic structure with or without interposition of a heteroatom) and a polyfluoro compound in which hydrogen atoms bound to the carbon atom of the fluoro-β-dicarbonyl compound are further substituted with ≥1 fluorine atoms is brought into contact with an acid-receiving agent.
      COPYRIGHT: (C)2005,JPO&NCIPI