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    Intermediates for the preparation of triazolinones
    23.
    发明授权
    Intermediates for the preparation of triazolinones 失效
    用于制备三唑啉酮的中间体

    公开(公告)号：US5639891A

    公开(公告)日：1997-06-17

    申请号：US528375

    申请日：1995-09-14

    Applicant: Karl-Heinz Linker ,  Wilhelm Haas ,  Kurt Findeisen ,  Hans-Joachim Diehr

    Inventor： Karl-Heinz Linker ,  Wilhelm Haas ,  Kurt Findeisen ,  Hans-Joachim Diehr

    IPC: C07D249/12

    CPC classification number: C07D249/12

    Abstract: The invention relates to a new process and new intermediates for the preparation of triazolinones of the general formula (I) ##STR1## in which R.sup.1 represents in each case optionally substituted alkyl or cycloalkyl andR.sup.2 represents amino or in each case optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkylamino, dialkylamino, cycloalkyl, cycloalkylalkyl or phenyl, and to new intermediates for the preparation of triazolinones, many of which are known and which can be used as intermediates for the preparation of herbicides and insecticides.

    Abstract translation: 本发明涉及用于制备通式（I）的三唑啉酮的新方法和新中间体，其中R 1表示在每种情况下为任选取代的烷基或环烷基，R 2表示氨基或在各种情况下任选取代 烷基，烯基，炔基，烷氧基，烷基氨基，二烷基氨基，环烷基，环烷基烷基或苯基，以及用于制备三唑啉酮的新中间体，其中许多是已知的，可用作制备除草剂和杀虫剂的中间体。

    Process and intermediates for the preparation of triazolinones
    25.
    发明授权
    Process and intermediates for the preparation of triazolinones 失效
    用于制备三唑啉酮的方法和中间体

    公开(公告)号：US5508420A

    公开(公告)日：1996-04-16

    申请号：US347985

    申请日：1994-12-05

    Applicant: Wilhelm Haas ,  Karl-Heinz Linker ,  Kurt Findeisen

    Inventor： Wilhelm Haas ,  Karl-Heinz Linker ,  Kurt Findeisen

    IPC: C07D249/12 ,  C07D249/14

    CPC classification number: C07D249/12

    Abstract: The invention relates to a new process and to new intermediates for the preparation of triazolinones, most of which are known, of the general formula (I) ##STR1## in which R.sup.1 and R.sup.2 have the meanings given in the application, and which can be used as intermediates for the preparation of herbicides and insecticides.

    Abstract translation: 本发明涉及新方法和用于制备三唑啉酮的新中间体，其中大部分是通式（I）的化合物，其中R 1和R 2具有本申请中给出的含义，以及 其可以用作制备除草剂和杀虫剂的中间体。

    Process for the preparation of acyl cyanides
    26.
    发明授权
    Process for the preparation of acyl cyanides 失效
    酰基氰的制备方法

    公开(公告)号：US4302583A

    公开(公告)日：1981-11-24

    申请号：US33606

    申请日：1979-04-25

    Applicant: Kurt Findeisen ,  Karl-Heinz Linker

    Inventor： Kurt Findeisen ,  Karl-Heinz Linker

    IPC: B01J31/02 ,  B01J27/00 ,  B01J27/26 ,  B01J31/00 ,  B01J31/04 ,  C07B61/00 ,  C07C20060101 ,  C07C67/00 ,  C07C253/00 ,  C07C255/16 ,  C07C255/17 ,  C07C255/31 ,  C07C255/38 ,  C07C255/40 ,  C07C255/45 ,  C07C255/56 ,  C07D207/10 ,  C07D235/04 ,  C07D253/06 ,  C07D307/30

    CPC classification number: C07C253/20 ,  C07C253/30

    Abstract: Novel process for the preparation of a monomeric acyl cyanide of the general formula ##STR1## in which R represents optionally substituted alkyl with up to 8 carbon atoms, optionally substituted cycloalkyl with 3 to 12 carbon atoms, optionally substituted aryl or an optionally substituted 5-membered or 6-membered heterocyclic radical, which optionally can be fused with a benzene ring,which process comprises heating the corresponding dimeric acyl cyanide of the general formula ##STR2## in which R has the meaning stated above, to a temperature of from 50.degree. to 300.degree. C. in the presence of a compound having a basic reaction and rapidly removing the monomeric acyl cyanide (I) formed from the reaction mixture.

    Abstract translation: 用于制备通式为（I）的单体酰基氰的新方法，其中R表示任选取代的具有至多8个碳原子的烷基，任选取代的具有3至12个碳原子的环烷基，任选取代的芳基或任选地 取代的5元或6元杂环基团，其任选地可以与苯环稠合，该方法包括将相应的通式为其中R具有上述含义的二羧酰基氰化物加成到 在具有碱性反应的化合物存在下，温度为50-300℃，并快速除去由反应混合物形成的单体酰基氰（I）。

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