METODO PARA LA ELABORACION DE CARBOXILATOS DE DIFLUORMETILPIRAZOLILO.

    公开(公告)号:ES2338281T3

    公开(公告)日:2010-05-05

    申请号:ES07822162

    申请日:2007-11-02

    Applicant: BASF SE

    Abstract: Método para la preparación de carboxilatos de pirazol-4-ilo sustituidos con difluormetilo de la fórmula general (I), **(Ver fórmula)** donde R1 representa alquilo de C1-C8, cicloalquilo de C3-C8, alcoxi de C1-C4-alquilo de C1-C4, cicloalcoxi de C3-C8-alquilo de C1-C4, alquenilo de C2-C8 o representa opcionalmente bencilo sustituido por 1, 2 ó 3 sustituyentes Ry1 seleccionados independientemente uno de otro entre alquilo de C1-C4, alcoxi de C1-C4 o nitro; y R2 representa hidrógeno, alquilo de C1-C4, bencilo o fenilo; los dos sustituyentes mencionados de último pueden estar sin sustituir o sustituidos por 1, 2 ó 3 sustituyentes Ry2 seleccionados independientemente uno de otro entre halógeno, CN, nitro, alquilo de C1-C4, haloalquilo de C1-C4, alcoxi de C1-C4 o haloalcoxi de C1-C4; por el cual se hace reaccionar a) un compuesto de la fórmula general (II) **(Ver fórmula)** en la cual X representa flúor, cloro o bromo, R1 posee uno de los significados previamente indicados y R4 representa alquilo de C1-C8, cicloalquilo de C3-C8, alquenilo de C2-C8, bencilo o fenilo, reacciona con un compuesto de silano de la fórmula general R3nSiCl(4-n), en la cual n representa 1, 2 ó 3 y los sustituyentes R3 se seleccionan independientemente uno de otro entre alquilo de C1-C8 o fenilo, y con un metal que se selecciona entre los metales de los grupos 1, 2, 3, 4 y 12 del sistema periódico y tiene un potencial redox de menos de -0,7 V, respecto de un electrodo patrón de hidrógeno (a 25ºC y 101,325 kPa), y b) la mezcla de reacción del paso a) reacciona con un compuesto de la fórmula general (III) (III)R2HN-NH2 en la cual R2 tiene uno de los significados previamente indicados.

    42.
    发明专利
    未知

    公开(公告)号:AT464285T

    公开(公告)日:2010-04-15

    申请号:AT03720529

    申请日:2003-04-25

    Applicant: BASF SE

    Abstract: A process is described for preparing 3-trifluoromethylphenyl 4-cyanobenzyl ketone by reacting a C 1 -C 2 -alkyl 3-trifluoromethylbenzoate with 4-tolunitrile in an aprotic polar solvent or an aprotic polar solvent mixture in the presence of at least an equimolar amount of a base which is selected from potassium alkoxides of primary C 1 -C 4 -alkanols.

    PROCESS FOR PREPARING ALKYL 2-ALKOXYMETHYLENE-4,4-DIFLUORO-3-OXOBUTYRATES

    公开(公告)号:CA2715668A1

    公开(公告)日:2009-09-03

    申请号:CA2715668

    申请日:2009-02-27

    Applicant: BASF SE

    Abstract: A process for preparing alkyl 2-alkoxymethylene-4,4-difluoro-3-oxobutyrates (VI) where R is methyl or ethyl, from crude reaction mixtures of alkyl 4,4-difluoroacetoacetates (I) by a) reacting alkyl acetate (II), RO M alkoxide (III), where M is a sodium or potassium ion, and alkyl difluoroacetate (IV), without additional solvent to form an enolate (V), b) releasing the corresponding alkyl 4,4-difluoroacetoacetate (I) from the enolate (V) by means of acid, c) removing the salt formed from cation M and acid anion as a solid and d) converting (I), without isolation from the crude reaction mixture, to the alkyl 2-alkoxymethylene-4,4-difluoro-3-oxobutyrate (VI), and the use of (VI) for preparing 1-methyl-3-difluoromethyl-pyrazol-3-ylcarboxyates (VII).

    Process for preparing substituted biphenyls

    公开(公告)号:AU2007267055A1

    公开(公告)日:2007-12-06

    申请号:AU2007267055

    申请日:2007-05-31

    Applicant: BASF SE

    Abstract: A process for preparing substituted biphenyls of the formula I in which the substituents are defined as follows: X is fluorine or chlorine; R1 is nitro, amino or NHR3; R2 is cyano, nitro, halogen, C1-C6-alkyl, C1-C-6-alkenyl, C1-C6-alkynyl, C1-C6-alkoxy, C1-C6-haloalkyl, C1-C6-alkylcarbonyl or phenyl; R3 is C1-C4-alkyl, C1-C4-alkenyl or C1-C4-alkynyl; n is 1, 2 or 3, where in case that n is 2 or 3, the R.sup.2 radicals may also be different, which comprises reacting the compound of the formula II in which Hal is halogen and X and R1 are as defined above, in the presence of a base and of a palladium catalyst selected from the group of:3 a) palladium-triarylphosphine or -trialkylphosphine complex with palladium in the zero oxidation state, b) salt of palladium in the presence of triarylphospine or trialkylphosphine as a complex ligand or c) metallic palladium, optionally applied to support, in the presence of triarylphosphine or trialkylphosphine, in a solvent, with a diphenylborinic acid (III) in which R2 and n are as defined above, where the triarylphosphines or trialkylphosphines used may be substituted.

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