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公开(公告)号:DE19824089A1
公开(公告)日:1999-12-02
申请号:DE19824089
申请日:1998-05-29
Applicant: BASF AG
Inventor: GUETTES BERND , SANDER MICHAEL , MURRAR IMBRIDT , WINKLER JUERGEN
Abstract: New isocyanate (NCO) prepolymers (I) are obtained by reacting (a) organic isocyanates with (b) components containing H-acid compounds at 20-90 deg C, in which component (b) is a mixture of (b1) difunctional alcohol(s), (b2) trifunctional alcohol(s), (b3) stabilizer(s) and optionally (b4) polyols and reaction of (a) and (b) is carried out in vinyl monomer(s). An Independent claim is also included for the preparation of prepolymers (I) in this way.
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公开(公告)号:DK1517906T3
公开(公告)日:2007-07-16
申请号:DK03760593
申请日:2003-06-06
Applicant: BASF AG
Inventor: NOACK RAINER , SANDER MICHAEL , HENNINGSEN MICHAEL
IPC: C07D405/06 , C07D521/00
Abstract: The present invention relates to a process for the preparation of 1,2,4-triazol-1-ylmethyloxiranes of the formula I in which A and B are identical or different and, independently of one another, are C 1 -C 4 -alkyl, phenyl-C 1 -C 2 -alkyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl or phenyl, where the phenyl radical can carry one to three substituents chosen from the group: halogen, nitro, C 1 -C 4 -alkyl, C l -C 4 -alkyloxy, phenoxy, amino, C 1 -C 2 -haloalkyl or phenylsulfonyl, which comprises reacting a) an oxirane of the formula II in which A and B have the meanings given above and L is a nucleophilically substitutable leaving group, with 4-amino-1,2,4-triazole of the formula III to give 4-amino-1,2,4-triazolium salts of the formula IV and b) deaminating the 4-amino-1,2,4-triazolium salts IV with alkali metal nitrites and acid or organic nitrites to give 1,2,4-triazol-1-ylmethyloxiranes of the formula I, and to 4-aminotriazolium salts of the formula IV as intermediates.
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公开(公告)号:NZ536848A
公开(公告)日:2007-05-31
申请号:NZ53684803
申请日:2003-06-06
Applicant: BASF AG
Inventor: NOACK RAINER , SANDER MICHAEL , HENNINGSEN MICHAEL
IPC: C07D405/06
Abstract: A method for the production of 1,2,4-triazol-1-yl-methyl-oxiranes of formula (I) is disclosed, wherein A and B are the same or different and independently represent C1-C4-alkyl, phenyl-C1-C2-alkyl, C3-C6-cycloalkyl, C3-C6-cycloalkenyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl or phenyl, wherein the phenyl radical can contain 1 to 3 substituents selected form the group: halogen, nitro, C1-C4-alkyl, C1-C4-alkyloxy, phenoxy, amino, C1-C2-halogenalkyl or phenylsulfonyl, wherein the method comprises: (a) reacting an oxirane of formula (II) wherein A and B have the above mentioned meaning and L represents a nucleophilically substitutable leaving group, with 4-amino-1,2,4-triazole of formula (III), to form 4-amino-1,2,4-triazolium salts of formula (IV), and (b) deaminating the 4-amino-1,2,4-triazolium salts (IV) with alkali metal nitrites and acid or organic nitrites to obtain 1,2,4-triazol-1-yl-methyl-oxiranes of formula (I).
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公开(公告)号:AT358127T
公开(公告)日:2007-04-15
申请号:AT03760593
申请日:2003-06-06
Applicant: BASF AG
Inventor: NOACK RAINER , SANDER MICHAEL , HENNINGSEN MICHAEL
IPC: C07D405/06 , C07D521/00
Abstract: The present invention relates to a process for the preparation of 1,2,4-triazol-1-ylmethyloxiranes of the formula I in which A and B are identical or different and, independently of one another, are C 1 -C 4 -alkyl, phenyl-C 1 -C 2 -alkyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl or phenyl, where the phenyl radical can carry one to three substituents chosen from the group: halogen, nitro, C 1 -C 4 -alkyl, C l -C 4 -alkyloxy, phenoxy, amino, C 1 -C 2 -haloalkyl or phenylsulfonyl, which comprises reacting a) an oxirane of the formula II in which A and B have the meanings given above and L is a nucleophilically substitutable leaving group, with 4-amino-1,2,4-triazole of the formula III to give 4-amino-1,2,4-triazolium salts of the formula IV and b) deaminating the 4-amino-1,2,4-triazolium salts IV with alkali metal nitrites and acid or organic nitrites to give 1,2,4-triazol-1-ylmethyloxiranes of the formula I, and to 4-aminotriazolium salts of the formula IV as intermediates.
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公开(公告)号:PL375212A1
公开(公告)日:2005-11-28
申请号:PL37521203
申请日:2003-06-06
Applicant: BASF AG
Inventor: NOACK RAINER , SANDER MICHAEL , HENNINGSEN MICHAEL
IPC: C07D405/06 , C07D521/00
Abstract: The present invention relates to a process for the preparation of 1,2,4-triazol-1-ylmethyloxiranes of the formula I in which A and B are identical or different and, independently of one another, are C 1 -C 4 -alkyl, phenyl-C 1 -C 2 -alkyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl or phenyl, where the phenyl radical can carry one to three substituents chosen from the group: halogen, nitro, C 1 -C 4 -alkyl, C l -C 4 -alkyloxy, phenoxy, amino, C 1 -C 2 -haloalkyl or phenylsulfonyl, which comprises reacting a) an oxirane of the formula II in which A and B have the meanings given above and L is a nucleophilically substitutable leaving group, with 4-amino-1,2,4-triazole of the formula III to give 4-amino-1,2,4-triazolium salts of the formula IV and b) deaminating the 4-amino-1,2,4-triazolium salts IV with alkali metal nitrites and acid or organic nitrites to give 1,2,4-triazol-1-ylmethyloxiranes of the formula I, and to 4-aminotriazolium salts of the formula IV as intermediates.
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公开(公告)号:ES2236524T3
公开(公告)日:2005-07-16
申请号:ES02738069
申请日:2002-05-14
Applicant: BASF AG
Inventor: NOACK RAINER , SANDER MICHAEL , KAISER REINHARD
IPC: C07D405/00 , C07D405/06
Abstract: Procedimiento para la purificación de isómeros de triazolilmetiloxirano de la fórmula general I en la que A y B son iguales o diferentes y significan, independientemente entre sí, alquilo con 1 a 4 átomos de carbono, fenil-alquilo con 1 a 2 átomos de carbono, cicloalquilo con 3 a 6 átomos de carbono, cicloalquenilo con 3 a 6 átomos de carbono, tetrahidropiranilo, tetrahidrofuranilo, dioxanilo o fenilo, pudiendo portar el resto fenilo uno a tres substituyentes seleccionados a partir del grupo: halógeno, nitro, alquilo con 1 a 4 átomos de carbono, alquiloxi con 1 a 4 átomos de carbono, fenoxi, amino, alquilo halogenado con 1 a 2 átomos de carbono o fenilsulfonilo, que se obtienen mediante reacción de un oxirano de la fórmula II en la que A y B poseen el significado citado anteriormente, y L representa un grupo saliente reemplazable por vía nucleófila, con a) 1, 2, 4-triazol (IIIa) y un equivalente molar de una base inorgánica, o b) 1, 2, 4-triazoluro de la fórmula IIIb, IIIa: Me = hidrógeno IIIb: Me = metal alcalino en la que Me representa un átomo metálico alcalino o un ión amonio cuaternario, en un disolvente dipolar, caracterizado porque, una vez concluida la reacción, se mezcla la disolución de reacción con un disolvente miscible con agua, y a continuación se precipita los isómeros de triazolilmetiloxirano con agua de manera fraccionada.
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公开(公告)号:ES2235053T3
公开(公告)日:2005-07-01
申请号:ES02740595
申请日:2002-05-14
Applicant: BASF AG
Inventor: SANDER MICHAEL , NOACK RAINER , KAISER REINHARD
IPC: C07D405/06 , C07D521/00
Abstract: Procedimiento para la obtención de triazolilmetiloxiranos de la **fórmula** en la que A y B son iguales o diferentes y significan, independientemente entre sí, alquilo con 1 a 4 átomos de carbono, fenil-alquilo con 1 a 2 átomos de carbono, cicloalquilo con 3 a 6 átomos de carbono, cicloalquenilo con 3 a 6 átomos de carbono, tetrahidropiranilo, tetrahidrofuranilo, dioxanilo o fenilo, pudiendo portar el resto fenilo uno a tres substituyentes seleccionados a partir del grupo: halógeno, nitro, alquilo con 1 a 4 átomos de carbono, alcoxi con 1 a 4 átomos de carbono, fenoxi, amino, alquilo halogenado con 1 a 2 átomos de carbono o fenilsulfonilo, mediante reacción de un oxirano, en la que A y B poseen el significado citado anteriormente, y L representa un grupo saliente substituible por vía nucleófila, con a) 1, 2, 4-triazol (IIIa) y un equivalente molar de una base inorgánica o b) un 1, 2, 4-triazoluro de la **fórmula** Me = hidrógeno (IIIb): Me = metal alcalino en la que Me representa un átomode metal alcalino o un ión amonio cuaternario, caracterizado porque se lleva a cabo el triazolado en un disolvente dipolar aprótico bajo secado azeotrópico simultáneo, de modo que su contenido en compuestos con OH ácidos asciende a menos de un 0,5%, y/o cuyo contenido en compuestos con NH ácidos asciende a menos de un 2,5%.
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公开(公告)号:DE19908793C2
公开(公告)日:2002-05-08
申请号:DE19908793
申请日:1999-03-01
Applicant: BASF AG
Inventor: SANDER MICHAEL , MURRAR IMBRIDT , GUETTES BERND
IPC: C07C263/18 , C08G18/70 , C08G18/40
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公开(公告)号:DE19857409A1
公开(公告)日:2000-06-15
申请号:DE19857409
申请日:1998-12-12
Applicant: BASF AG
Inventor: SANDER MICHAEL , PENZEL ULRICH , SCHWARZ HANS VOLKMAR , STROEFER ECKHARD , STUETZER DIETER , MUELLER JOERN , MAURER MARKUS
IPC: B01J10/00 , B01J19/00 , B01J19/24 , B01J19/26 , C07C209/36 , C07C211/51 , C07B43/04 , C07C209/32
Abstract: The production of amines (I) by hydrogenation of nitro compounds (II), carried out in a vertical reactor with length greater than its diameter. It has a spray at the top for introducing educts and reaction mixture and an outlet through which the reaction mixture is pumped into an external cycle. The circulation is reversed in the lower zone of the reactor.
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公开(公告)号:ZA200500607B
公开(公告)日:2006-07-26
申请号:ZA200500607
申请日:2005-01-21
Applicant: BASF AG
Inventor: HENNINGSEN MICHAEL , NOACK RAINER , SANDER MICHAEL
IPC: C07D405/06 , C07D20060101 , C07D521/00
Abstract: The present invention relates to a process for the preparation of 1,2,4-triazol-1-ylmethyloxiranes of the formula I in which A and B are identical or different and, independently of one another, are C 1 -C 4 -alkyl, phenyl-C 1 -C 2 -alkyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl or phenyl, where the phenyl radical can carry one to three substituents chosen from the group: halogen, nitro, C 1 -C 4 -alkyl, C l -C 4 -alkyloxy, phenoxy, amino, C 1 -C 2 -haloalkyl or phenylsulfonyl, which comprises reacting a) an oxirane of the formula II in which A and B have the meanings given above and L is a nucleophilically substitutable leaving group, with 4-amino-1,2,4-triazole of the formula III to give 4-amino-1,2,4-triazolium salts of the formula IV and b) deaminating the 4-amino-1,2,4-triazolium salts IV with alkali metal nitrites and acid or organic nitrites to give 1,2,4-triazol-1-ylmethyloxiranes of the formula I, and to 4-aminotriazolium salts of the formula IV as intermediates.
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