VERBESSERTES VERFAHREN ZUR HERSTELLUNG VON HALOGENMETHYLCYCLOPROPANEN UND BESONDERS REINE HALOGENMETHYLCYCLOPROPANE
    2.
    发明公开
    VERBESSERTES VERFAHREN ZUR HERSTELLUNG VON HALOGENMETHYLCYCLOPROPANEN UND BESONDERS REINE HALOGENMETHYLCYCLOPROPANE 失效
    改进方法卤素甲基环丙烷和特别PURE卤素甲基丙CYCLO的制备

    公开(公告)号:EP0882004A1

    公开(公告)日:1998-12-09

    申请号:EP97903252.0

    申请日:1997-02-10

    申请人: BAYER AG

    IPC分类号: C07C17 C07C22

    摘要: In an improved process for the production of halogen methyl cyclopropanes of formula (I) in which Hal is chlorine or bromine and R1 to R5 are mutually independently hydrogen, optionally substituted C¿1?-C10 alkyl or optionally substituted C6-C10 aryl, the corresponding hydroxymethyl propanes are mixed with chlorine or bromine and an organic phosphorus compound, and chlorine or bromine is reacted in an excess of at least 5 mol % (in relation to te hydroxymethyl cyclopropane). It is thus possible to obtain highly pure products containing little 1-halogen-3-butene.

    摘要翻译: 本发明涉及一种用于halogenomethylcyclopropanes的制备方法。

    VERFAHREN ZUR HERSTELLUNG VON NAPHTHYRIDINVERBINDUNGEN UND NEUE ZWISCHENPRODUKTE
    4.
    发明公开
    VERFAHREN ZUR HERSTELLUNG VON NAPHTHYRIDINVERBINDUNGEN UND NEUE ZWISCHENPRODUKTE 失效
    用于生产萘啶和新中间体

    公开(公告)号:EP0935600A1

    公开(公告)日:1999-08-18

    申请号:EP97913157.0

    申请日:1997-10-17

    申请人: BAYER AG

    IPC分类号: C07D211 C07D213 C07D471

    摘要: An advantageous method of producing naphthyridine compounds of formulae (Ia) to (1c) wherein R means hydrogen or C1-C4 alkyl, Ar means possibly substituted phenyl, Hal means independently fluorine, chlorine or bromine, and n stands for 1, 2 or 3, whereby a halogenated nicotinic, isonicotinic or picolinic acid is made to react with an amino acrylic acid ester to obtain a halogenated 2-nicotinoyl-, isonicotinoyl- or picolinoyl-3-aminoacrylate which is made to react with an optionally substituted aniline to obtain a halogenated 2-nicotinoyl-, isonicotinoyl- or picolinoyl-3-aminoacrylate which contains an amino group corresponding to the optionally substituted aniline. The second halogenated 2-nicotinoyl-, isonicotinoyl- or picolinoyl-3-aminoacrylate is cyclized by adding an acid scavenger to a compound of formulae (Ia) to (Ic) with R = C1-C4 alkyl and, in the case of production of a compound of formulae (Ia) to (Ic) with R = H, the compound of the formulae (Ia) to (Ic) with R = C1-C4 alkyl is saponified.