111.
    发明专利
    未知

    公开(公告)号:DE19942299A1

    公开(公告)日:2001-03-08

    申请号:DE19942299

    申请日:1999-09-04

    Applicant: BASF AG

    Abstract: The invention relates to a method for producing aliphatic, cycloaliphatic, araliphatic and aromatic monoisocyanates and oligoisocyanates by phosgenating the corresponding primary amines at normal pressure. The inventive method is characterized in that: a) a catalytic quantity of a monoisocyanate (isocyanate a) is placed in an inert solvent with phosgene; b) the primary amine is added, and; c) the reaction mixture obtained thereby is reacted with phosgene.

    Method for producing methylglycine-N,N-diethanoic acid-trialkali metal salts with a low by-product content

    公开(公告)号:AU2006245816B2

    公开(公告)日:2011-04-14

    申请号:AU2006245816

    申请日:2006-05-02

    Applicant: BASF AG

    Abstract: The invention relates to a process for preparing low-by-product, light-color methylglycine-N,N-diacetic acid tri(alkali metal) salt by alkaline hydrolysis of methylglycinediacetonitrile (MGDN), comprising the steps in the sequence (a) to (f): (a) mixing of MGDN with aqueous alkali at a temperature of ≦̸30° C.; (b) allowing the aqueous alkaline MGDN suspension to react at a temperature in the range from 10 to 30° C. over a period of from 0.1 to 10 h to form a solution; (c) allowing the solution from step (b) to react at a temperature in the range from 30 to 40° C. over a period of from 0.1 to 10 h; (d) optionally allowing the solution from step (c) to react at a temperature in the range from 50 to 80° C. over a period of from 0.5 to 2 h; (e) optionally allowing the solution from step (c) or (d) to react at a temperature in the range from 110 to 200° C. over a period of from 5 to 60 min; (f) hydrolysis and removal of ammonia of the solution obtained in step (c), (d) or (e) by stripping at a temperature of from 90 to 105° C.

    116.
    发明专利
    未知

    公开(公告)号:NO20075532L

    公开(公告)日:2008-02-04

    申请号:NO20075532

    申请日:2007-11-02

    Applicant: BASF AG

    Abstract: The invention relates to a process for preparing low-by-product, light-color methylglycine-N,N-diacetic acid tri(alkali metal) salt by alkaline hydrolysis of methylglycinediacetonitrile (MGDN), comprising the steps in the sequence (a) to (f): (a) mixing of MGDN with aqueous alkali at a temperature of ≦̸30° C.; (b) allowing the aqueous alkaline MGDN suspension to react at a temperature in the range from 10 to 30° C. over a period of from 0.1 to 10 h to form a solution; (c) allowing the solution from step (b) to react at a temperature in the range from 30 to 40° C. over a period of from 0.1 to 10 h; (d) optionally allowing the solution from step (c) to react at a temperature in the range from 50 to 80° C. over a period of from 0.5 to 2 h; (e) optionally allowing the solution from step (c) or (d) to react at a temperature in the range from 110 to 200° C. over a period of from 5 to 60 min; (f) hydrolysis and removal of ammonia of the solution obtained in step (c), (d) or (e) by stripping at a temperature of from 90 to 105° C.

    METODO PARA PRODUCIR SALES DE METAL TRIALCALINO DE ACIDO METILGLICIN - N, N - DIETANOICO CON UN BAJO CONTENIDO DE PRODUCTO SECUNDARIO.

    公开(公告)号:MX2007013702A

    公开(公告)日:2008-01-21

    申请号:MX2007013702

    申请日:2006-05-02

    Applicant: BASF AG

    Abstract: La invencion se relaciona con un metodo para producir una sal de metal trialcalino de acido metilglicina-N,N-dietanoico de color claro con un bajo contenido de producto secundario, mediante la hidrolisis alcalina de diacetonitrilo de metilglicina, el metodo comprende pasos que se llevan a cabo en el orden (a) a (f): (a) mezclado del diacetonitrilo de metilglicina con una lejia de alcali acuoso a una temperatura de = 30 degree C; (b) la suspension de diacetonitrilo de metilglicina alcalina acuosa luego se hace reaccionar a una temperatura que varia entre 10 y 30 degree C durante un periodo de 0.1 a 10 horas, para formar una solucion; (c) la solucion obtenida en el paso (b) luego se hace reaccionar a una temperatura que varia entre 30 y 40 degree C durante un periodo de 0.1 a 10 horas; (d) opcionalmente la solucion obtenida en el paso (c) se hace reaccionar a una temperatura que varia entre 50 y 80 degree C durante un periodo de entre 0.5 y 2 h; (e) opcionalmente la solucion obtenida en el paso (c) o (d) se hace reaccionar a una temperatura que varia entre 110 y 200 degree C durante un periodo de entre 5 y 60 minutos; (f) hidrolisis y aislamiento de amoniaco de la solucion obtenida en el paso (c), (d) o (e) separando a una temperatura de entre 90 y 105 degree C.

    119.
    发明专利
    未知

    公开(公告)号:DE50107832D1

    公开(公告)日:2005-12-01

    申请号:DE50107832

    申请日:2001-02-28

    Applicant: BASF AG

    Abstract: The invention relates to a method for producing chlorocarboxylic acid chlorides of formula (I), wherein R and R , independently from one another, mean a hydrogen atom, an organic radical containing carbon, a halogen, a nitro or cyano group and Y means an alkylene chain having 1 to 10 carbon atoms in the chain which is unsubstituted or is substituted by organic radicals that contain carbon, by halogen, nitro and/or cyano groups, whereby the alkylene chain can be interrupted by an ether-, thioether-, tertiary amino- or keto group, whereby the organic radicals of Y and/or R and/or R can be connected to one another and thereby form a non-aromatic system, whereby said radicals contain carbon, by converting a lactone of formula (II), wherein R , R and Y have the aforementioned meanings, using a hydrogen chloride and phosgene in the presence of a catalyst. Hydrogen chloride is added before and/or while phosgene is added. The hydrogen chloride is only introduced at a temperature of at least 60 DEG C. A pyridine compound is used as the catalyst.

    METHOD FOR PRODUCING CARBOXYLIC ACID CHLORIDES

    公开(公告)号:HU224531B1

    公开(公告)日:2005-10-28

    申请号:HU0104207

    申请日:1999-10-29

    Applicant: BASF AG

    Abstract: The invention relates to a process for the preparation of acid chlorides by reaction of carboxylic acids, carboxylic anhydrides, cyclic carboxylic esters or sulfonic acids with phosgene in the presence of a catalytic amount of a compound from the group consisting of N,N,N',N'-tetrasubstituted amidinium halides (I), N,N,N'-trisubstituted amidinium hydrohalides (II) and N,N,N'-trisubstituted amidines (III).

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