111.
    发明专利
    未知

    公开(公告)号:BRPI0808555A2

    公开(公告)日:2014-08-19

    申请号:BRPI0808555

    申请日:2008-02-27

    Applicant: BASF SE

    Abstract: This invention relates to a process for preparing substituted phenylhydrazines of the formula I wherein R has the meaning as indicated in the description, comprising reacting a dichlorofluorobenzene of the formula II with a hydrazine source selected from hydrazine, hydrazine hydrate and acid addition salts of hydrazine and optionally being carried out in the presence of at least one organic solvent.

    METHOD FOR MANUFACTURING ARYL CARBOXAMIDES.

    公开(公告)号:MX317270B

    公开(公告)日:2014-01-20

    申请号:MX2010011276

    申请日:2009-05-06

    Applicant: BASF SE

    Abstract: A process for preparing arylcarboxamides of the formula (I) where Ar=a mono- to trisubstituted phenyl, pyridyl or pyrazolyl ring, where the substituents are selected from halogen, C1-C4-alkyl and C1-C4-haloalkyl; M=thienyl or phenyl, which may bear a halogen substituent; Q=direct bond, cyclopropylene, fused bicyclo[2.2.1]heptane or bicyclo[2.2.1]heptene ring; R1=hydrogen, halogen, C1-C6-alkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, mono- to trisubstituted phenyl, where the substituents are selected from halogen and trifluoromethylthio, or cyclopropyl; by reacting an acid chloride of the formula (II) with an arylamine (III) in a suitable nonaqueous solvent, wherein, in the absence of an auxiliary base, a) the acid chloride (II) is initially charged, b) a pressure of from 0 to 700 mbar is established, c) the arylamine (III) is metered in an approximately stoichiometric amount and d) the product of value is isolated.

    Método para la preparación de ésteres halosustituidos de ácido 2-(aminometiliden)-3-oxobutírico

    公开(公告)号:ES2386940T3

    公开(公告)日:2012-09-06

    申请号:ES09738223

    申请日:2009-04-30

    Applicant: BASF SE

    Abstract: Método para la preparación de compuestos de la fórmula (I), **Fórmula**dondeR1 representa alquilo de C1-C6, haloalquilo de C1-C6, alquenilo de C2-C6, cicloalquilo de C3-C10 o bencilo, en cuyocaso ambos residuos mencionados de último están sin sustituir o tienen 1, 2 o 3 sustituyentes seleccionadosindependientemente entre sí de halógeno, CN, nitro, alquilo de C1-C4, haloalquilo de C1-C4, alcoxi de C1-C4 yhaloalcoxi de C1-C4;R2 y R3, independientemente entre sí, representan alquilo de C1-C6, haloalquilo de C1-C6, alquenilo de C2-C6,cicloalquilo de C3-C10 o bencilo, en cuyo caso los dos residuos mencionados de último están sin sustituir o tienen o1, 2 o 3 sustituyentes seleccionados independientemente entre sí de entre halógeno, CN, nitro, alquilo de C1-C4,haloalquilo de C1-C4, alcoxi de C1-C4 y haloalcoxi de C1-C4; oR2 conjuntamente con R3 y el átomo de nitrógeno al cual ambos residuos están enlazados representan un residuoheterocíclico de 5 a 10 miembros opcionalmente sustituidos, el cual puede comprender, además del átomo denitrógeno, 1, 2 o 3 heteroátomos más seleccionados entre O, N y S en calidad de miembros de anillo;R4 representa hidrógeno, flúor o cloro; yX1 y X2, independientemente entre sí, representan flúor o cloro;En el cual se hace reaccionar un compuesto de la fórmula (II),donde R1, R2 y R3 tienen uno de los significados dados previamente; con un compuesto de la fórmula X1X2R420 CC(>=O)-F en presencia de al menos un fluoruro de metal alcalino o de metal alcalino térreo.

    Process for preparing difluoromethylpyrazolyl carboxylates

    公开(公告)号:AU2007316081B2

    公开(公告)日:2012-04-26

    申请号:AU2007316081

    申请日:2007-11-02

    Applicant: BASF SE

    Abstract: The present invention relates to a process for preparing difluoromethyl-substituted pyrazol-4-yl carboxylates of the formula (I) in which R is C-C-alkyl, C-C-cycloalkyl, C-C-alkoxy-C-C-alkyl, etc.; and R is hydrogen, C-C-alkyl, benzyl or phenyl, wherein a) a compound of the general formula (II) in which X is fluorine, chlorine, or bromine, R has one of the definitions given above, and R is C-C-alkyl, C-C-cycloalkyl, C-C-alkenyl, benzyl or phenyl, is reacted with a silane compound of the general formula R SiClin which n is 1, 2 or 3 and the substituents R are each independently selected from C-C-alkyl and phenyl, and with a metal which is selected from the metals of groups 1, 2, 3, 4 and 12 of the periodic table and has a redox potential of less than -0.7 V, based on a standard hydrogen electrode (at 25°C and 101.325 kPa); and b) the reaction mixture from step a) is reacted with a compound of the general formula (III) in which R has one of the definitions given above.

    СПОСОБ ПОЛУЧЕНИЯ ДИФТОРМЕТИЛПИРАЗОЛИЛКАРБОКСИЛАТОВ

    公开(公告)号:UA97498C2

    公开(公告)日:2012-02-27

    申请号:UAA200904967

    申请日:2007-11-02

    Applicant: BASF SE

    Abstract: Данноеизобретениекасаетсяспособаполучениядифторметилзамещенныхпиразол-4-илкарбоксилатовформулы I, (I)вкоторойRозначает C-C-алкил, С-С-циклоалкил, С-С-алкокси-С-С-алкили т.п.; иRозначаетводород, С-С-алкил, бензилилифенил,причема) соединениеобщейформулы II, (II)вкоторой X означаетфтор, хлорилибром, Rимеетодноизприведенныхпреждезначенийи RозначаетС-С-циклоалкил, С-С-алкенил, бензилилифенил,взаимодействуетс силановымсоединениемобщейформулы RSiCl, вкоторой n означает 1, 2 или 3 изаместители R, независимодруготдругавыбраныизС-С-алкилаилифенила, ис металлом, которыйвыбранизметаллов 1, 2, 3, 4 и 12 группыПериодическойсистемыэлементови имеетокислительно-восстановительныйпотенциалменьшечем-0,7 V, вперечислениинанормальныйводородныйэлектро

    119.
    发明专利
    未知

    公开(公告)号:AT520667T

    公开(公告)日:2011-09-15

    申请号:AT08761025

    申请日:2008-06-13

    Applicant: BASF SE

    Abstract: The present invention relates to a process for preparing 3-difluoromethyl-Substituted pyrazole compounds of the formula (I) in which R1 is H, halogen, nitro, C1-C8-alkyl, C1-C8-haloalkyl, C3-C8-cycloalkyl, phenyl, naphthyl, hetaryl, cyano, —C(═O)—OR1a, —C(═O)—NR1bR1c, —C(═O)—SR1d or —C(═S)—SR1e; R2 is H, C1-C4-alkyl, benzyl or phenyl; R3 is H, halogen, C1-C8-alkoxy, C1-C8-haloalkoxy, C3-C8-cycloalkoxy, C2-C8-alkenyloxy, C1-C8-alkylthio, C1-C8-haloalkylthio, C3-C8-cyclo-alkylthio or C2-C8-alkenylthio; compounds of the formula (II.a) or (II.b), in which R1 and R3 each have one of the definitions given above; R4 is halogen, —OR4a, —SR4a, —O—SO2—R4a or an —NR4bR4c group; R5 and R6 are each C1-C8-alkyl, C1-C8-haloalkyl, C3-C8-cycloalkyl, benzyl or phenyl, or, together with the nitrogen atom to which they are bonded, are a 3- to 8-membered heterocycle; Lewis acid adducts of compounds of the formula (II.b); the use of compounds of the formula (II.a) or (II.b) and of the Lewis acid adducts for preparing compounds of the formula (I) or (VI); and to a process for converting such compounds to the corresponding 3-difluoro-pyrazol-4-ylcarboxylic acids.

    PROCEDIMIENTO PARA LA OBTENCION DE ARILCARBOXAMIDAS.

    公开(公告)号:MX2010011276A

    公开(公告)日:2010-11-09

    申请号:MX2010011276

    申请日:2009-05-06

    Applicant: BASF SE

    Abstract: Procedimiento para la obtención de arilcarboxamidas de la fórmula (I) (ver formula (I)) en la que Ar = es un anillo fenilo, piridilo o pirazolilo mono a trisustituido, seleccionando los sustituyentes de halógeno, C1-C4-alquilo y C1-C4-halógenoalquilo; M = es tienilo o fenilo, que puede llevar un sustituyente halógeno; Q = es un enlace directo, ciclopropileno, un anillo biciclo(2.2.1]heptano o biciclo[2.2.1]hepteno anelado; R1 = es hidrógeno, halógeno, C1-C6-alquilo, C1-C4-alcoxi, C1-C4-halógenoalcoxi, fenilo mono a trisustituido, seleccionando los sustituyentes de halógeno y trifluorometiltio, o ciclopropilo; transformando un cloruro de ácido de la fórmula (II) (ver fórmula (II) con una arilamina (III) (ver fórmulas (III)) en un solvente no soluble en agua apropiado, en cuyo procedimiento a) se presenta el cloruro de ácido (II) como carga inicial en presencia de una base auxiliar, b) se regula una presión de 0 hasta 700 mbar, c) se dosifica la arilamina (III) en cantidad aproximadamente estequiométrica y d) se aísla el producto de valor.

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