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    • 13. 发明授权
    • Preparation of amines
    • 胺的制备
    • US06462236B2
    • 2002-10-08
    • US09983307
    • 2001-10-24
    • Shelue LiangFrank FunkeArthur Höhn
    • Shelue LiangFrank FunkeArthur Höhn
    • C07C20926
    • C07C209/26C07C211/29
    • Amines of the formula (I) R1R2CH—NR3R4  (I) where R1, R2, R3 and R4 are each, independently of one another, hydrogen, straight-chain or branched C1-C12-alkyl, C3-C12-cycloalkyl, C6-C10-aryl or C7-C11-aralkyl, where at least one of the radicals R1 and R2 is aryl or aralkyl whose aromatic unit is substituted by at least one halogen, are prepared by catalytic, hydrogenative amination of carbonyl compounds of the formula (II) or alcohols of the formula (III) R1—C(═O)—R2  (II) R1—CH(OH)—R2  (III) by means of nitrogen compounds of the formula (IV) HNR3R4  (IV) where R1 to R4 are as defined above, in the presence of Co- and/or Ni-containing catalysts, in the additional presence of solid acid cocatalysts and in the absence of organic sulfur compounds.
    • 式(I)的胺其中R 1,R 2,R 3和R 4各自独立地为氢,直链或支链C 1 -C 12 - 烷基,C 3 -C 12 - 环烷基,C 6 -C 10 - 芳基或C 7 -C 12 - C 11 - 芳烷基,其中基团R 1和R 2中的至少一个是其芳族单元被至少一个卤素取代的芳基或芳烷基,其通过式(II)的羰基化合物的催化,氢化胺化或式 (III)通过其中R 1至R 4如上所定义的式(Ⅳ)的氮化合物在存在Co和/或Ni的催化剂的情况下,在固体酸助催化剂的另外存在下,在不存在 有机硫化合物。
    • 14. 发明授权
    • Method for producing cyclopentanone
    • 环戊酮生产方法
    • US06429339B1
    • 2002-08-06
    • US09700365
    • 2000-11-15
    • Shelue LiangRolf FischerFrank SteinJoachim Wulff-Döring
    • Shelue LiangRolf FischerFrank SteinJoachim Wulff-Döring
    • C07C4500
    • B01J23/10C07C45/48C07C49/395
    • A process for preparing cyclopentanone by reacting adipic esters of the formula R1OOC—(CH2)4—COOR2  I where R1 and R2 are each alkyl having from 1 to 12 carbon atoms, cycloalkyl having 5 or 6 carbon atoms, aralkyl or aryl and R2 may additionally be hydrogen, in the presence of oxidic catalysts comprises reacting adipic esters of the formula I having less than 5% by weight of by-products other than adipic esters in the gas phase in the presence of water, a carrier gas and a) from 0.01 to 10% by weight of at least one metal oxide selected from the first or second main group of the periodic table or from the group of the rare earth metals on titanium dioxide or zirconium dioxide as catalyst support, or b) from 0.01 to 50% by weight of at least one metal oxide selected from the second main group of the periodic table on zink oxide as catalyst support.
    • 通过使式R 1和R 2的己二酸酯反应制备环戊酮的方法各自是在氧化催化剂存在的情况下,可以另外为氢,其中R 1和R 2各自为具有1至12个碳原子的烷基,具有5或6个碳原子的环烷基或芳基, 包括使式I的己二酸酯在水,载气的存在下,在气相中具有小于5重量%的除己二酸酯之外的副产物,和(ii)0.01至10重量%的至少一种金属 氧化物,其选自周期表的第一或第二主族,或者来自稀土金属的二氧化钛或二氧化锆的组,作为催化剂载体,orb)为0.01至50重量%的至少一种选自 氧化锌作为催化剂载体的周期表第二主要组。