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    • 5. 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。