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    2.
    发明专利
    未知

    公开(公告)号：BR0016214A

    公开(公告)日：2002-09-17

    申请号：BR0016214

    申请日：2000-11-27

    Applicant: BASF AG

    Inventor： STAMM ARMIN ,  TZ ROLAND G ,  TZ NORBERT G ,  HENKELMANN JOCHEM ,  KNEUPER HEINZ-JOSEF ,  WOLF BERND

    IPC: C07C51/58 ,  C07B61/00 ,  C07C51/09 ,  C07C57/76 ,  C07C51/00

    Abstract: The invention relates to a method for producing o-choromethyl benzenecarbonyl chlorides of formula (I), wherein R -R can be the same or different and stand for hydrogen, C1-C4-alkyl, halogen or trifluoromnethyl, by converting benzocondensed lactones of formula (II), wherein R -R have the aforementioned meaning, with gaseous or liquid phosgene and the dimers or trimers thereof. The inventive method is characterized in that the conversion is carried out in the presence of catalytical amounts of a Lewis acid and catalytical amounts of a phosgenation catalyst

    5.
    发明专利
    未知

    公开(公告)号：BR9915423A

    公开(公告)日：2001-08-07

    申请号：BR9915423

    申请日：1999-11-12

    Applicant: BASF AG

    Inventor： GRAMMENOS WASSILIOS ,  SAUTER HUBERT ,  GYPSER ANDREAS ,  BAYER HERBERT ,  TZ NORBERT G ,  TZ ROLAND G

    IPC: C07B61/00 ,  C07C249/12 ,  C07C251/60

    Abstract: The process for preparing alkenyl-substituted bis(oxime ether) derivatives of the formula Iwhere:R1 is unsubstituted C1-C4-alkyl or C2-C4-alkenyl-, C2-C4-alkynyl- or phenyl-substituted methyl;R2, R4 independently of one another are hydrogen or methyl;R3, R5 independently of one another are hydrogen or C1-C4-alkyl, trifluoromethyl or phenyl andX is -C(=CHCH3)-COOCH3,-C(=CHOCH3)-COOCH3,-C(=NOCH3)-COOCH3,-C(=NOCH3)-CONHCH3 or-N(OCH3)-COOCH3,and intermediates which are obtainable by this process are described. Alkenyl-substituted bis(oxime ether) derivatives of the formula I are described in the literature as interesting crop protection agents.

    6.
    发明专利
    未知

    公开(公告)号：BRPI0414410A

    公开(公告)日：2006-11-14

    申请号：BRPI0414410

    申请日：2004-09-10

    Applicant: BASF AG

    Inventor： GRAMMENOS WASSILIOS ,  BLETTNER CARSTEN ,  MUELLER BERND ,  GEWEHR MARKUS ,  BLASCO JORDI TORMO I ,  GROTE THOMAS ,  RHEINHEIMER JOAQUIM ,  SCHOFER PETER ,  SCHIEWECK FRANK ,  GLER ANJA SWCHW ,  WAGNER OLIVER ,  TZ NORBERT G ,  STRATHMANN SIEGFRIED ,  FL ULRICH SCH ,  SCHERER MARIA ,  STIERL REINHARD

    IPC: C07D213/42 ,  C07D215/12 ,  C07D401/12 ,  C07D409/12

    Abstract: Sulfonamides of the formula I where the substituents are as follows: R 1 is hydrogen, alkyl, alkoxy, alkenyl or alkynyl; and R 2 , R 3 , R 4 , R 5 are hydrogen, halogen, alkyl, alkoxy or halomethyl; R 2 and R 3 together may also form a phenyl, cyclopentyl or cyclohexyl ring, it being possible for these rings to carry two groups R 2 ' and R 3 ', R 2 ', R 3 ' are hydrogen, halogen, alkyl, alkoxy or halomethyl; in case a), if R 2 , R 3 , R 4 and R 5 are hydrogen: X is phenyl substituted by a group C(R 6 )-NOR 7 , where R 6 is alkyl and R 7 is alkyl, benzyl, alkenyl, haloalkyl, haloalkenyl, alkynyl or haloalkynyl; and in case b), if at least one of the groups R 2 , R 3 , R 4 and R 5 is not hydrogen: X is phenyl, naphthyl or a five- or six-membered saturated, or partially unsaturated or aromatic heterocycle which is attached via a carbon atom and contains one to four heteroatoms from the group consisting of O, N and S, where X may be substituted according to the description; Processes for preparing these compounds, compositions comprising them and their use for controlling phytopathogenic harmful fungi.

    7.
    发明专利
    未知

    公开(公告)号：BR0206449A

    公开(公告)日：2003-12-30

    申请号：BR0206449

    申请日：2002-01-15

    Applicant: BASF AG

    Inventor： VOLK THORSTEN ,  PUHL MICHAEL ,  ZAGAR CYRILL ,  LOCHTMAN RENE ,  TZ NORBERT G ,  HAMPRECHT GERHARD

    IPC: C07D231/20

    Abstract: The invention relates to a method of preparing 1-alkyl-3-aryl-5-difluoromethoxy-1H-pyrazoles of the formula (I), wherein aryl represents a mono- or polysubstituted phenyl ring, and R 1 represents C 1 -C 4 alkyl. The inventive method is characterized by reacting, in a first reaction step, a beta-ketoester of the general formula (II) with hydrazine and by successively reacting the reaction product obtained with chlorodifluoromethane and a compound R 1 -L, wherein R 1 has the meanings indicated above and L represents the leaving group of a nucleophilic displacement reaction.

    8.
    发明专利
    未知

    公开(公告)号：BR9915492A

    公开(公告)日：2001-08-07

    申请号：BR9915492

    申请日：1999-11-06

    Applicant: BASF AG

    Inventor： MAYWALD VOLKER ,  STEINMETZ ADRIAN ,  RACK MICHAEL ,  TZ NORBERT G ,  TZ ROLAND G ,  HENKELMANN JOCHEM ,  BECKER HEIKE ,  BAYETO JUAN JOSE AISCAR

    IPC: C07D231/20

    Abstract: The invention relates to a process for preparing 1-substituted 5- and/or 3-hydroxypyrazoles of the formulae I and IIin which R1 is C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C6-cycloalkyl or C1-C4-alkoxy, where these groups may be substituted by halogen, C1-C4-alkoxy, phenoxy, C1-C6-alkoxycarbonyl, C1-C6-alkylthiocarbonyl or by a cyclic ring system having 3-14 ring atoms, which comprises reactingan alkyl 3-alkoxyacrylate of the formula IIIin which R2, R3 independently of one another are C1-C6-alkyl or C3-C6-cycloalkyl with a hydrazine of the formula IVin which R1 is as defined abovea) at a pH of 6-11 to give 5-hydroxypyrazoles of the formula I orb) at a pH of 11-14 to give 3-hydroxypyrazoles of the formula II.

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