Zpusob prípravy 1-substituovaných 5-nebo 3-hydroxypyrazolu

    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

    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.

    METHOD FOR PRODUCING 1-SUBSTITUTED 5- AND/OR 3-HYDROXYPYRAZOLES

    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

    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.

    65.
    发明专利
    未知

    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

    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.

    66.
    发明专利
    未知

    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

    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.

    METHOD FOR PRODUCING CHLOROCARBOXYLIC ACID CHLORIDES

    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

    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.

    69.
    发明专利
    未知

    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

    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.

    СПОСІБ ОДЕРЖАННЯ N-ЗАМІЩЕНИХ 3-ГІДРОКСИПІРАЗОЛІВ

    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

    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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