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公开(公告)号:CZ301828B6
公开(公告)日:2010-07-07
申请号:CZ20011713
申请日:1999-11-06
Applicant: BASF AG
Inventor: MAYWALD VOLKER , STEINMETZ ADRIAN , RACK MICHAEL , GOETZ NORBERT , GOETZ ROLAND , HENKELMANN JOCHEM , BECKER HEIKE , BAYETO JUAN JOSE AISCAR
IPC: C07D231/20
Abstract: Je popsán zpusob prípravy 1-substituovaných 5- a/nebo 3-hydroxypyrazolu vzorcu I a II, který zahrnuje reakci (a) alkylvinyletheru vzorce V, s fosgenem vzorce VIa, "difosgenem" vzorce VIb nebo "trifosgenem" vzorce VIc za vzniku acylchloridu vzorce VII, (b) jeho konverzi na odpovídající 3-alkoxyakryloylchlorid vzorce VIII odstranením chlorovodíku a (c) esterifikaci tohoto produktu alkoholem vzorce IX, za vzniku odpovídajícího alkyl-3-alkoxyakrylatu vzorce III, a reakci tohoto alkyl-3-alkoxyakrylatu vzorce III s hydrazinem vzorce IV, (d) pri pH 6 až 11 za vzniku 5-hydroxypyrazolu vzorce I nebo (e) pri pH 11 až 14 za vzniku 3-hydroxypyrazolu vzorce II. Význam všech substituentu je uveden v popise.
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公开(公告)号:PL205283B1
公开(公告)日:2010-03-31
申请号:PL34875199
申请日:1999-11-06
Applicant: BASF AG
Inventor: MAYWALD VOLKER , STEINMETZ ADRIAN , RACK MICHAEL , GOETZ NORBERT , GOETZ ROLAND , HENKELMANN JOCHEM , BECKER HEIKE , AISCAR BAYETO JUAN JOSE
IPC: C07D231/20
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公开(公告)号:HU224721B1
公开(公告)日:2006-01-30
申请号:HU0104504
申请日:1999-11-06
Applicant: BASF AG
Inventor: MAYWALD VOLKER , STEINMETZ ADRIAN , RACK MICHAEL , GOETZ NORBERT , GOETZ ROLAND , HENKELMANN JOCHEM , BECKER HEIKE , AISCAR BAYETO JUAN JOSE
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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公开(公告)号:DE59909774D1
公开(公告)日:2004-07-22
申请号:DE59909774
申请日:1999-12-01
Applicant: BASF AG
Inventor: NEIDLEIN ULF , GOETZ NORBERT , MISSLITZ ULF , GOETZ ROLAND , BAUMANN ERNST , VON DEYN WOLFGANG , KUDIS STEFFEN , LANGEMANN KLAUS , MAYER GUIDO , WITSCHEL MATTHIAS , OTTEN MARTINA , WESTPHALEN KARL-OTTO , WALTER HELMUT
IPC: C07D231/12 , A01N43/56 , A01N43/74 , A01N43/78 , A01N43/80 , C07B61/00 , C07D403/10 , C07D413/10 , C07D417/10
Abstract: The present invention relates to 1-cycloalkylpyrazolylbenzoyl derivatives of the formula Iwherein all variables are as defined in the specification, their agriculturally useful salts, processes for their preparation, and for the use of these compounds or compositions comprising them, for controlling undesirable plants.
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公开(公告)号:DE50005355D1
公开(公告)日:2004-03-25
申请号:DE50005355
申请日:2000-11-27
Applicant: BASF AG
Inventor: GOETZ ROLAND , GOETZ NORBERT , KEIL MICHAEL , WOLF BERND , STEINMETZ ADRIAN , STAMM ARMIN , HENKELMANN JOCHEM
Abstract: A process for preparing o-chloromethylbenzoyl chlorides of the formula I,in which R to R can be identical or different and are hydrogen, C1-C4-alkyl, halogen or trifluoromethyl, by reacting benzo-fused lactones of the formula II,in which R to R are as defined above, with thionyl chloride, which comprises carrying out the reaction in the presence of catalytic amounts of boric acid, boric anhydride, borate, boronic acid or boronic acid esters and catalytic amounts of a quaternary ammonium salt is described.
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公开(公告)号:AT259770T
公开(公告)日:2004-03-15
申请号:AT00987303
申请日:2000-11-27
Applicant: BASF AG
Inventor: GOETZ ROLAND , GOETZ NORBERT , KEIL MICHAEL , WOLF BERND , STEINMETZ ADRIAN , STAMM ARMIN , HENKELMANN JOCHEM
Abstract: A process for preparing o-chloromethylbenzoyl chlorides of the formula I,in which R to R can be identical or different and are hydrogen, C1-C4-alkyl, halogen or trifluoromethyl, by reacting benzo-fused lactones of the formula II,in which R to R are as defined above, with thionyl chloride, which comprises carrying out the reaction in the presence of catalytic amounts of boric acid, boric anhydride, borate, boronic acid or boronic acid esters and catalytic amounts of a quaternary ammonium salt is described.
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公开(公告)号:DE59906901D1
公开(公告)日:2003-10-09
申请号:DE59906901
申请日:1999-11-06
Applicant: BASF AG
Inventor: MAYWALD VOLKER , STEINMETZ ADRIAN , RACK MICHAEL , GOETZ NORBERT , GOETZ ROLAND , HENKELMANN JOCHEM , BECKER HEIKE , AISCAR BAYETO JUAN JOSE
IPC: C07B61/00 , C07D231/20
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公开(公告)号:HU0300215A2
公开(公告)日:2003-07-28
申请号:HU0300215
申请日:2001-02-28
Applicant: BASF AG
Inventor: CLOSS FRIEDRICH , GOETZ ROLAND , HENKELMANN JOCHEM , KNEUPER HEINZ-JOSEF , STAMM ARMIN
Abstract: Production of chloroalkanoyl chlorides (I) with a (substituted) 1-10 carbon (hetero)alkylene chain, by reacting a lactone (II) with a chlorinating agent in the presence of a chlorination catalyst, is carried out in the presence of a boron compound. Production of chloroalkanoyl chlorides of formula (I) with a (substituted) 1-10 carbon (hetero)alkylene chain, by reacting a lactone of formula (II) with a chlorinating agent in the presence of a chlorination catalyst, is carried out in the presence of a boron compound. [Image] R1>, R2>H or R; R : halo, nitro, cyano or an organic group containing carbon; Y : optionally R-substituted 1-10 C alkylene, which may have a (thio)ether, tertiary amino or keto group in the chain; and R groups on Y, R1> and/or R2>can be linked to form a non-aromatic system.
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公开(公告)号:DE59709989D1
公开(公告)日:2003-06-05
申请号:DE59709989
申请日:1997-12-04
Applicant: BASF AG
Inventor: VOGELBACHER JOSEF , KEIL MICHAEL , KLINTZ RALF , WAHL JOSEPH , WINGERT HORST , KOENIG HARTMANN , RACK MICHAEL , GOETZ ROLAND , TELES HENRIQUE
IPC: C07D231/20 , C07D231/22
Abstract: PCT No. PCT/EP97/06780 Sec. 371 Date Jun. 14, 1999 Sec. 102(e) Date Jun. 14, 1999 PCT Filed Dec. 4, 1997 PCT Pub. No. WO98/27062 PCT Pub. Date Jun. 25, 1998A process is described for preparing N-substituted 3-hydroxypyrazoles of the formula I where R1 is unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, aryl or heteroaryl and R2, R3 are hydrogen, cyano, halogen and unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, aryl or heteroaryl, by oxidizing a corresponding pyrazolidin-3-one.
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公开(公告)号:UA53678C2
公开(公告)日:2003-02-17
申请号:UA99074135
申请日:1997-12-04
Applicant: BASF AG
Inventor: KEIL MICHAEL , WINGERT HORST , RACK MICHAEL , GOETZ ROLAND
IPC: C07D231/20 , C07D231/22
Abstract: Данийвинахідвідноситьсядоспособуодержання N-заміщених 3-гідроксипіразолівформулиІ вякій R1 означаєС1-С10алкіл, С2-С10алкеніл, С2-С10алкініл, С3-С10циклоалкіл, арил, вибранийз фенілуі нафтилу; гетероарил, вибранийз фурилу, тієнілу, піролілу, ізоксазолілу, ізотіазолілу, піразолілу, оксазолілу, імідазолілу, піридилу, піридазинілу, піримідинілуаботриазинілу, і R2, R3 означаютьводень, ціано, галогені С1-С10алкіл, С2-С10алкеніл, С2-С10алкініл, С3-С10циклоалкіл; арил, вибранийз фенілуі нафтилу; гетероарил, вибранийз фурилу, тієнілу, піролілу, ізоксазолілу, ізотіазолілу, піразолілу, оксазолілу, імідазолілу, піридилу, піридазинілу, піримідинілуаботриазинілу, причомузамісники R1, R2 і R3 єінертнимив умовахреакції, шляхомокисленняпіразолідин-3-ону.
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