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    Method for the hydrodehalogenation of halogenated meta-cresols
    1.
    发明申请
    Method for the hydrodehalogenation of halogenated meta-cresols 失效
    卤代间甲酚加氢脱卤的方法

    公开(公告)号：US20070149829A1

    公开(公告)日：2007-06-28

    申请号：US10583019

    申请日：2004-12-07

    申请人： Michael Pies ,  Klaus Schonauer ,  Volker Hassmann ,  Hermann Uhr

    发明人： Michael Pies ,  Klaus Schonauer ,  Volker Hassmann ,  Hermann Uhr

    IPC分类号： C07C39/24

    CPC分类号： C07C37/00 ,  C07C39/07

    摘要： The present process serves for the hydrodehalogenation of halogenated meta-cresols of the formula (I) in which the R1 to R4 radicals are each as defined in the description, and is characterized in that halogenated meta-cresols of the formula (I) are contacted with a catalyst which has been prepared by applying one or more salts of palladium and/or platinum and optionally copper salts to an aluminum oxide or titanium oxide support material, together with hydrogen, at temperatures between 100 and 250° C.

    摘要翻译： 本发明方法用于式（I）的卤代间甲酚的加氢脱卤，其中R 1至R 4基团各自如说明书中所定义，并且 其特征在于将式（I）的卤代间甲酚与通过将一种或多种钯和/或铂盐和任选的铜盐一起施加到氧化铝或氧化钛载体材料上一起制备的催化剂接触 与氢气在100和250℃之间。

    Method for the hydrodehalogenation of halogenated meta-cresols
    2.
    发明授权
    Method for the hydrodehalogenation of halogenated meta-cresols 失效
    卤代间甲酚加氢脱卤的方法

    公开(公告)号：US07399890B2

    公开(公告)日：2008-07-15

    申请号：US10583019

    申请日：2004-12-07

    申请人： Michael Pies ,  Klaus Schönauer ,  Volker Hassmann ,  Hermann Uhr

    发明人： Michael Pies ,  Klaus Schönauer ,  Volker Hassmann ,  Hermann Uhr

    IPC分类号： C07C39/24 ,  C07C37/00

    CPC分类号： C07C37/00 ,  C07C39/07

    摘要： The present process serves for the hydrodehalogenation of halogenated meta-cresols of the formula (I) in which the R1 to R4 radicals are each as defined in the description, and is characterized in that halogenated meta-cresols of the formula (I) are contacted with a catalyst which has been prepared by applying one or more salts of palladium and/or platinum and optionally copper salts to an aluminum oxide or titanium oxide support material, together with hydrogen, at temperatures between 100 and 250° C.

    摘要翻译： 本发明方法用于式（I）的卤代间甲酚的加氢脱卤，其中R 1至R 4基团各自如说明书中所定义，并且 其特征在于将式（I）的卤代间甲酚与通过将一种或多种钯和/或铂盐和任选的铜盐一起施加到氧化铝或氧化钛载体材料上一起制备的催化剂接触 与氢气在100和250℃之间。

    PROCESS FOR PREPARING IODOPROPARGYL COMPOUNDS
    3.
    发明申请
    PROCESS FOR PREPARING IODOPROPARGYL COMPOUNDS 有权
    制备碘化物化合物的方法

    公开(公告)号：US20120330051A1

    公开(公告)日：2012-12-27

    申请号：US13390707

    申请日：2010-08-26

    申请人： Bernd Koop ,  Hermann Uhr ,  Wolfgang Gausing

    发明人： Bernd Koop ,  Hermann Uhr ,  Wolfgang Gausing

    IPC分类号： C07C269/06

    CPC分类号： C07C269/06 ,  C07C271/12

    摘要： Process for the preparation of iodopropargyl compounds of the formula (I), in which R is hydrogen, in each case optionally substituted C1-C20-alkyl, C2-C20 alkenyl, C6-C20-aryl or C3-C20-cycloalkyl and n is an integer from 1 to 6, characterized in that propargyl compounds of the formula (II) in which R and n have the above meaning, are reacted with iodine and/or metal iodides in the presence of a base and using chlorine.

    摘要翻译： 制备式（I）的碘代炔丙基化合物的方法，其中R是氢，在各种情况下是任选取代的C 1 -C 20 - 烷基，C 2 -C 20烯基，C 6 -C 20 - 芳基或C 3 -C 20 - 环烷基，n是 其特征在于其中R和n具有上述含义的式（II）的炔丙基化合物在碱的存在下与碘和/或金属碘化物反应，并使用氯。

    Fungicidal trisubstituted 1,2,4-triazine-3,5-diones
    6.
    发明授权
    Fungicidal trisubstituted 1,2,4-triazine-3,5-diones 失效
    杀真菌剂分解的1,2,4-三嗪-3,5-二酮

    公开(公告)号：US5096903A

    公开(公告)日：1992-03-17

    申请号：US644049

    申请日：1991-01-18

    申请人： Hermann Uhr ,  Arno Widdig ,  Dieter Berg ,  Gerd Hanssler

    发明人： Hermann Uhr ,  Arno Widdig ,  Dieter Berg ,  Gerd Hanssler

    IPC分类号： A01N43/707 ,  C07D253/06 ,  C07D253/075

    CPC分类号： C07D253/075 ,  A01N43/707

    摘要： Fungicidal trisubstituted 1,2,4-triazine-3,5-diones of the formula ##STR1## in which Ar represents optionally substituted aryl,R.sup.1 represents an optionally substituted aliphatic of cycloaliphatic radical andR.sup.2 represents an optionally substituted aliphatic radical.Many of the intermediates therefor where R.sup.2 is hydrogen and/or the 3-O is replaced by 3-S are also new.

    摘要翻译： 式（I）的杀真菌三取代的1,2,4-三嗪-3,5-二酮，其中Ar表示任选取代的芳基，R 1表示任选取代的脂环族基团，R 2表示任选取代的脂族基团。 其中R2是氢和/或3-O被3-S替代的许多中间体也是新的。

    Method for the production of substituted azoles
    10.
    发明申请
    Method for the production of substituted azoles 审中-公开
    制备取代的唑类的方法

    公开(公告)号：US20090306397A1

    公开(公告)日：2009-12-10

    申请号：US11921252

    申请日：2006-05-27

    申请人： Rainer Bruns ,  Hermann Uhr ,  Erasmus Vogl

    发明人： Rainer Bruns ,  Hermann Uhr ,  Erasmus Vogl

    IPC分类号： C07D257/04

    CPC分类号： C07D257/04

    摘要： The novel process for preparing substituted azoles allows compounds of the general formula (I) and/or their salts and/or their acid addition compounds in which the substituents R1 and R2, A and B are as defined in the description to be prepared in good yield and in a simple, economically favourable manner.

    摘要翻译： 制备取代的吡唑的新方法允许其中取代基R 1和R 2，A和B如说明书中所定义的通式（I）和/或其盐和/或其酸加成化合物的化合物制备成良好的 产量和简单，经济上有利的方式。