会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 3. 发明专利
    • Preparation of carbonyl compounds
    • 碳化合物的制备
    • JPS54148706A
    • 1979-11-21
    • JP5640378
    • 1978-05-12
    • Chisso Corp
    • TSUNODA KAZUOYOSHIZAWA SATORUFUKUI MASAHIRO
    • C07C45/54C07C45/00C07C67/00
    • PURPOSE: To obtain carbonyl compounds which are raw materials for solvents, perfumes, medicines, etc., in high yield, by the vapor-phase catalytic reacion of formic acid esters, which are by-products in the preparation of acids, etc. from aldehydes, in the presence of a specific metallic compound catalyst at a high temperature.
      CONSTITUTION: Carbonyl compounds of formula II are obtained by the vapor- phase catalytic reaction of formic esters of formula I (R
      1 is H, C
      1W10 alkyl or alkenyl; R
      2 is C
      1W10 alkyl, alkenyl, etc.) in the presence of a specific catalyst at a temperature of 200-450°C. An oxide of at least one kind of metal selected from the group of Sn, Bi, Fe, Cd and Mn is used as the catalyst. Furthermore, addition of 1W5 moles of water to 1 mole of formic acid ester improves life of the catalyst and selectivity. Even if a raw material with a low formic ester content of 20W30% is used, the reaction is possible.
      COPYRIGHT: (C)1979,JPO&Japio
    • 目的:通过甲酸酯的气相催化反应获得作为溶剂,香料,药物等原料的羰基化合物,其为酸的制备中的副产物等。 醛在特定的金属化合物催化剂存在下在高温下进行。 构成:式II的羰基化合物是通过式I的甲酸酯(R 1是H,C 1-10烷基或烯基; R 2是C 1-10烷基,烯基等)的气相催化反应得到的, 在200-450℃温度下的特定催化剂。 使用选自Sn,Bi,Fe,Cd和Mn中的至少一种金属的氧化物作为催化剂。 此外,向1摩尔甲酸酯中加入1-5摩尔水可改善催化剂的寿命和选择性。 即使使用20-30%的低甲酸酯含量的原料,也可以进行反应。
    • 10. 发明专利
    • PRODUCTION OF METALLOCENE COMPOUND
    • JPH07278168A
    • 1995-10-24
    • JP6588194
    • 1994-04-04
    • CHISSO CORP
    • YOSHIZAWA SATORUMATSUKAWA TETSUYANAKAMURA YUTAKA
    • C07F17/00C07F7/08
    • PURPOSE:To produce the subject different-kind coordination position silicon- crosslinking type metallocene compound of high purity in a high yield by a specified method. CONSTITUTION:(A) A mixture complex between a substituted cyclopentadiene of formula I [R to R each is H, a 1 to 4C alkyl, etc., provided that one or more of them is not H; the ring Cp is a cyclopentadienyl ring], a base of the formula, RpYqM [R is H, phenyl, etc.; Y 18 N, O, etc.; M is a alkaline (earth) metal; (p) is 1 or 2; (q) is 0 or 1] and a metal ion capturing agent and (B) a mixture complex between a cyclopentadiene compound of formula II (R to R each is phenyl, a 1 to 4C alkyl, etc.), the above-mentioned base and a metal capturing agent are initially prepared. The complexes A and B are then reacted with a dimethylhalosilane in an arbitrary order and a strong base is subsequently added to an ether-based solvent solution of the synthesized compound of formula III to obtain a product. A complexing solution prepared by dissolving an inert so vent dispersion of a compound of the formula, MX [M is a transition metal; X is a halogen; (v) is 3 to 5] in an etherbased solvent is finally reacted with the product, thus producing the objective compound of formula IV.