利索-全球专利检索

  1. 登录
  2. 注册

搜索结果

22 条记录 (耗时 0.022 秒)

    Preparation of 3-aminomethyl-3,5,5-trimethyl-cyclohexylamine
    4.
    发明授权
    Preparation of 3-aminomethyl-3,5,5-trimethyl-cyclohexylamine 失效
    3-氨基甲基-3,5,5-三甲基 - 环己胺的制备

    公开(公告)号：US5371292A

    公开(公告)日：1994-12-06

    申请号：US92029

    申请日：1993-07-15

    申请人： Franz Merger ,  Claus-Ulrich Priester ,  Tom Witzel ,  Gerhard Koppenhoefer ,  Wolfgang Harder

    发明人： Franz Merger ,  Claus-Ulrich Priester ,  Tom Witzel ,  Gerhard Koppenhoefer ,  Wolfgang Harder

    IPC分类号： B01J21/04 ,  B01J21/06 ,  B01J23/46 ,  B01J27/18 ,  C07B61/00 ,  C07C209/00 ,  C07C209/26 ,  C07C209/48 ,  C07C209/52 ,  C07C211/36 ,  C07C209/24

    CPC分类号： C07C209/48 ,  C07C209/26 ,  C07C2101/14

    摘要： A process for the preparation of 3-aminomethyl-3,5,5-trimethyl-cyclohexylamine from 3-cyano-3,5,5-trimethyl-cyclohexanone, wherein the following stages are carried out in discrete reaction chambers:a) the 3-cyano-3,5,5-trimethyl-cyclohexanone is reacted in a first reaction chamber with excess ammonia over an acidic metal oxide catalyst at a temperature of from 20.degree. to 150.degree. C. and a pressure of from 15 to 500 bar, andb) in a second reaction chamber, the reaction product from stage a) is hydrogenated with hydrogen at a temperature of from 60.degree. to 150.degree. C. and a pressure of from 50 to 300 bar in the presence of excess ammonia over a catalyst containing cobalt, nickel, ruthenium, and/or some other noble metal, which catalyst optionally contains a basic component or is supported by neutral or basic supporting material.

    摘要翻译： 从3-氰基-3,5,5-三甲基 - 环己酮制备3-氨基甲基-3,5,5-三甲基 - 环己胺的方法，其中以下步骤在离散反应室中进行：a）3 氰基-3,5,5-三甲基 - 环己酮在第一反应室中与过量的氨在酸性金属氧化物催化剂上在20至150℃的温度和15至500巴的压力下反应， 和b）在第二反应室中，在过量的氨在催化剂存在下，将氢气从60℃升至150℃，压力为50-300巴，在步骤a）中的反应产物被氢化 含有钴，镍，钌和/或一些其它贵金属，该催化剂任选地含有碱性组分或由中性或碱性载体材料负载。

    Preparation of 2-(3-aminopropyl)-cycloalkylamines
    6.
    发明授权
    Preparation of 2-(3-aminopropyl)-cycloalkylamines 失效
    2-（3-氨基丙基） - 环丙基胺的制备

    公开(公告)号：US5239120A

    公开(公告)日：1993-08-24

    申请号：US676087

    申请日：1991-03-27

    申请人： Franz Merger ,  Claus-Ulrich Priester ,  Gerhard Koppenhoefer ,  Wolfgang Harder ,  Tom Witzel ,  Helmut Lermer ,  Ulrich Koehler

    发明人： Franz Merger ,  Claus-Ulrich Priester ,  Gerhard Koppenhoefer ,  Wolfgang Harder ,  Tom Witzel ,  Helmut Lermer ,  Ulrich Koehler

    IPC分类号： B01J23/40 ,  B01J23/74 ,  B01J29/06 ,  C07B61/00 ,  C07C209/26 ,  C07C209/48 ,  C07C211/36

    CPC分类号： C07C209/48 ,  C07C209/26 ,  C07C2101/08 ,  C07C2101/14

    摘要： A process for the preparation of a 2-(3-aminopropyl)-cycloalkylamine of the general formula I ##STR1## in which the subscript n is an integer from 1 to 4, from a 2-(2-cyanoethyl)-cycloalkanone of the general formula II ##STR2## in which the subscript n has the meaning stated, wherein the following stages are carried out in discrete reaction chambers:a) the 2-(2-cyanoethyl)-cycloalkanone of formula II is reacted in a first reaction chamber with excess ammonia over an acidic heterogeneous catalyst at a temperature from 20.degree. to 150.degree. C. and a pressure of from 15 to 500 bar, andb) in a second reaction chamber, the reaction product from stage a) is hydrogenated at a temperature of from 60.degree. to 150.degree. C. and a pressure of from 50 to 300 bar in the presence of excess ammonia over a catalyst containing cobalt, nickel, ruthenium, and/or some other noble metal, which catalyst optionally contains a basic component or is supported on neutral or basic supporting material.

    摘要翻译： 2-（2-氰基乙基） - （2-氨基丙基） - 环烷基胺的制备方法，其中下标n为1至4的整数，通式I（I） 通式II（II）的环烷酮，其中下标n具有所述的含义，其中以下步骤在离散的反应室中进行：a）式II的2-（2-氰基乙基） - 环烷酮是 在酸性多相催化剂的第一反应室中，在第二反应室中，在20至150℃的温度和15至500巴的压力下，在第一反应室中与过量的氨反应，和b）在第二反应室中，反应产物从步骤a ）在过量氨的存在下在含有钴，镍，钌和/或一些其它贵金属的催化剂的温度下在60至150℃的温度和50至300巴的压力下氢化，该催化剂 可选地含有基本组分或者在中性或基础支撑材料上支撑。

    Joint preparation of 3-dialkylaminopropionitriles, bis-(2-cyanoethyl) ether and, if desired, ethylene-cyanohydrin
    7.
    发明授权
    Joint preparation of 3-dialkylaminopropionitriles, bis-(2-cyanoethyl) ether and, if desired, ethylene-cyanohydrin 失效
    联合制备3-二烷基氨基丙腈，双（2-氰基乙基）醚和（如果需要）乙烯 - 氰醇

    公开(公告)号：US4965362A

    公开(公告)日：1990-10-23

    申请号：US376373

    申请日：1989-07-06

    申请人： Franz Merger ,  Wolfgang Harder ,  Peter Hettinger ,  Claus-Ulrich Priester ,  Dieter Franz ,  Dieter Voges

    发明人： Franz Merger ,  Wolfgang Harder ,  Peter Hettinger ,  Claus-Ulrich Priester ,  Dieter Franz ,  Dieter Voges

    IPC分类号： C07C253/18 ,  C07C255/12 ,  C07C255/13 ,  C07C255/24

    CPC分类号： C07C255/12 ,  C07C255/13 ,  C07C255/24

    摘要： 3-Dialkylaminopropionitriles ##STR1## where R.sup.1 and R.sup.2 are each C.sub.1 -C.sub.4 -alkyl which may furthermore be bonded to form a 5-membered or 6-membered ring, bis-(2-cyanoethyl) ether IINC--CH.sub.2 --CH.sub.2 --O--CH.sub.2 --CH.sub.2 --CN IIand, if desired, ethylenecyanohydrin IIIHO--CH.sub.2 --CH.sub.2 --CN IIIare prepared jointly by a process in which(a) acrylonitrile and water are reacted in the presence of a base at from 60.degree. to 150.degree. C. to give a mixture of acrylonitrile, water and bis-(2-cyanoethyl) ether II, the base being a mineral base, a quaternary nitrogen base or a mixture of these,(b) this mixture is reacted at about 0.degree.-50.degree. C. with a dialkylamine of the general formula IV ##STR2## to give a mixture of water, a dialkylaminopropionitrile I and bis-(2-cyanoethyl) ether II, and this mixture is separated into its components and(c) if desired, the ether II obtained in proces stage (b) or an aqueous solution of this ether and/or the reacted mixtures containing this ether and obtained from process stage (a) or (b) is allowed to react at from 50.degree. to 150.degree. C. with the dialkylamine IV to give a mixture of a 3-dialkylaminopropionitrile I and ethylenecyanohydrin III, and, if desired, the said mixture is separated into its components.

    摘要翻译： 3-二烷基氨基丙腈其中R 1和R 2各自为可以连接形成5元或6元环的C 1 -C 4 - 烷基，双 - （2-氰基乙基）醚II NC-CH 2 -CH 2 - O-CH 2 -CH 2 -CN II和如果需要，乙烯基氰醇III HO-CH 2 -CH 2 -CN III通过以下方法共同制备，其中（a）丙烯腈和水在碱的存在下在60℃至 150℃，得到丙烯腈，水和双 - （2-氰基乙基）醚II的混合物，碱为矿物碱，季氮碱或它们的混合物，（b）该混合物在约0℃ 与二烷基胺（通式IV IV）反应，得到水，二烷基氨基丙腈I和双 - （2-氰基乙基）醚II的混合物，将该混合物分离成其组分，（c ）如果需要，在步骤阶段（b）中获得的醚II或该醚的水溶液和/或含有该醚的反应混合物从工艺步骤（a）或（b）获得， 使其与二烷基胺IV在50-150℃下反应，得到3-二烷基氨基丙腈I和乙基烯丙醇III的混合物，如果需要，将所述混合物分离成其组分。

    Preparation of caprolactam
    8.
    发明授权
    Preparation of caprolactam 失效
    己内酰胺的制备

    公开(公告)号：US4963672A

    公开(公告)日：1990-10-16

    申请号：US448899

    申请日：1989-12-12

    申请人： Franz Merger ,  Rolf Fischer ,  Wolfgang Harder ,  Claus-Ulrich Priester ,  Uwe Vagt

    发明人： Franz Merger ,  Rolf Fischer ,  Wolfgang Harder ,  Claus-Ulrich Priester ,  Uwe Vagt

    IPC分类号： B01J23/46 ,  C07B61/00 ,  C07D201/08 ,  C07D201/16

    CPC分类号： C07D201/08 ,  Y02P20/52

    摘要： Caprolactam is prepared in a process comprising the following steps:(a) reacting the 5-formylvaleric ester with liquid ammonia as reaction medium and hydrogen in the presence of a ruthenium catalyst in liquid phase at from 80.degree. to 140.degree. C. under a hydrogen partial pressure of from 40 to 100 bar,(b) replacing the reaction medium ammonia by an aromatic hydrocarbon having a boiling point of from 80.degree. to 240.degree. C. which is liquid under the reaction conditions,(c) heating the resulting mixture in liquid phase under superatmospheric pressure at 230.degree.-350.degree. C. to form caprolactam, and(d) isolating caprolactam from the resulting reaction mixture.

    摘要翻译： 己内酰胺以包括以下步骤的方法制备：（a）使5-甲酰基戊酸酯与液氨作为反应介质和氢在钌催化剂存在下在液相中在80-140℃下在氢气 分压为40〜100巴，（b）在反应条件下用沸点为80〜240℃的芳烃替代反应介质氨，（c）将所得混合物加热 液相在超大气压下在230-350℃下反应形成己内酰胺，和（d）从所得反应混合物中分离己内酰胺。