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公开(公告)号:DE59608206D1
公开(公告)日:2001-12-20
申请号:DE59608206
申请日:1996-06-03
Applicant: BASF AG
Inventor: DE KRAMER JAN , NEUMANN ULRICH , KLEIN ULRICH , MEIWALD MECHTILD , KRIEG WOLFGANG
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公开(公告)号:ES2139730T3
公开(公告)日:2000-02-16
申请号:ES94903822
申请日:1993-12-17
Applicant: BASF AG
Inventor: HARREUS ALBRECHT , GOTZ NORBER , MAYWALD VOLKER , RANG HARALD , MISSLITZ ULF , KLEIN ULRICH
IPC: C07C239/20 , C07C251/54 , C07C253/30 , C07C255/54 , C07C259/06
Abstract: PCT No. PCT/EP93/03597 Sec. 371 Date Jun. 6, 1995 Sec. 102(e) Date Jun. 6, 1995 PCT Filed Dec. 17, 1993 PCT Pub. No. WO94/14757 PCT Pub. Date Jul. 7, 1994Hydroxylamine ethers I I (where X is NO2, CN, halogen, alkyl or haloalkyl, Y is H, NO2, CN, halogen, alkyl or haloalkyl, n is 0-2 or 1-4 where Y and all radicals X are halogen and Alk is unsubstituted or substituted alkylene) and their salts with mineral acids or strong organic acids are prepared by reacting either a hydroximino compound II II (where R1 is alkyl, R2 is alkyl or alkoxy or R1+R2 form an alkylene chain) in the presence of an alkali metal hydroxide, alkali metal alcoholate, alkali metal bicarbonate or alkali metal carbonate as the base, or the corresponding anion II directly, with an alkylating agent III III (where R3 is unsubstituted or substituted alkyl or unsubstituted or substituted phenyl) to give an oximino derivative IV IV said derivative is cleaved by means of a mineral acid or a strong organic acid to give the salt of I and, if desired, the latter is converted by means of a base into the free compound I. The hydroxylamine ethers I are intermediates for crop protection agents and drugs.
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公开(公告)号:AT186046T
公开(公告)日:1999-11-15
申请号:AT94903822
申请日:1993-12-17
Applicant: BASF AG
Inventor: HARREUS ALBRECHT , GOETZ NORBER , MAYWALD VOLKER , RANG HARALD , MISSLITZ ULF , KLEIN ULRICH
IPC: C07C239/20 , C07C251/54 , C07C253/30 , C07C255/54 , C07C259/06
Abstract: PCT No. PCT/EP93/03597 Sec. 371 Date Jun. 6, 1995 Sec. 102(e) Date Jun. 6, 1995 PCT Filed Dec. 17, 1993 PCT Pub. No. WO94/14757 PCT Pub. Date Jul. 7, 1994Hydroxylamine ethers I I (where X is NO2, CN, halogen, alkyl or haloalkyl, Y is H, NO2, CN, halogen, alkyl or haloalkyl, n is 0-2 or 1-4 where Y and all radicals X are halogen and Alk is unsubstituted or substituted alkylene) and their salts with mineral acids or strong organic acids are prepared by reacting either a hydroximino compound II II (where R1 is alkyl, R2 is alkyl or alkoxy or R1+R2 form an alkylene chain) in the presence of an alkali metal hydroxide, alkali metal alcoholate, alkali metal bicarbonate or alkali metal carbonate as the base, or the corresponding anion II directly, with an alkylating agent III III (where R3 is unsubstituted or substituted alkyl or unsubstituted or substituted phenyl) to give an oximino derivative IV IV said derivative is cleaved by means of a mineral acid or a strong organic acid to give the salt of I and, if desired, the latter is converted by means of a base into the free compound I. The hydroxylamine ethers I are intermediates for crop protection agents and drugs.
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公开(公告)号:BR9609533A
公开(公告)日:1999-02-23
申请号:BR9609533
申请日:1996-07-02
Applicant: BASF AG
Inventor: KOENIG HARTMANN , GOETZ NORBERT , KLEIN ULRICH , ELLER KARSTEN
IPC: C07D231/20 , C07D231/22 , C07D401/04
Abstract: PCT No. PCT/EP96/02891 Sec. 371 Date Jan. 8, 1998 Sec. 102(e) Date Jan. 8, 1998 PCT Filed Jul. 2, 1996 PCT Pub. No. WO97/03969 PCT Pub. Date Feb. 6, 1997N-substituted 3-hydroxypyrazoles of the formula I where R1 is unsubstituted or substituted alkyl, aryl or heteroaryl and R2, R3 is hydrogen, cyano, halogen or unsubstituted or substituted alkyl, aryl or heteroaryl, are prepared by oxidation of a corresponding pyrazolidin-3-one with atmospheric oxygen in the presence of a metal salt in an essentially pH-neutral medium.
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公开(公告)号:AT165812T
公开(公告)日:1998-05-15
申请号:AT94924726
申请日:1994-07-08
Applicant: BASF AG
Inventor: KLEIN ULRICH , BUSCHMANN ERNST , KEIL MICHAEL , GOETZ NORBERT , HARREUS ALBRECHT
IPC: C07C239/20
Abstract: PCT No. PCT/EP94/02239 Sec. 371 Date Jan. 11, 1996 Sec. 102(e) Date Jan. 11, 1996 PCT Filed Jul. 8, 1994 PCT Pub. No. WO95/04032 PCT Pub. Date Feb. 9, 1995Preparation of O-substituted hydroxylammonium salts IR1-CHX-O-NH2.HL(I)(L=halogen, hydrogensulfate; X=H, alkyl; R1=unsubst. or subst. phenyl, thienyl, furanyl, pyrrolyl or -CR2=CR3R4; R2, R3, R4=H, halogen or alkyl) by reaction of an acetone oxime O-allyl or -O-benzyl ether II (II) with water and a mineral acid H-L with continuous removal of the acetone formed in this process, by carrying out the hydrolysis batchwise at 0 DEG -50 DEG C. and under a pressure of 10-500 mbar is described. The O-substituted hydroxylammonium salts I are intermediates for plant protection agents and pharmaceuticals.
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公开(公告)号:MX9800412A
公开(公告)日:1998-04-30
申请号:MX9800412
申请日:1996-07-02
Applicant: BASF AG
Inventor: KOENIG HARTMANN , GOETZ NORBERT , KLEIN ULRICH , ELLER KARSTEIN
IPC: C07D231/20 , C07D231/22 , C07D401/04
Abstract: Los 3-hidroxipirazoles N-substituidos de la formula (I), en donde, R1 es alquilo, arilo o heteroarilo no substituido o substituido, y R2 y R3 es hidrogeno, ciano, halogeno o alquilo, arilo o heteroarilo no substituido o substituido se preparan mediante oxidacion de una pirazolidin-3-ona correspondiente.
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公开(公告)号:ZA964811B
公开(公告)日:1997-12-08
申请号:ZA964811
申请日:1996-06-07
Applicant: BASF AG
Inventor: KRAMER JACOBUS JAN DE , NEUMANN ULRICH , KLEIN ULRICH , MEIWALD MECHTILD , KRIEG WOLFGANG
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公开(公告)号:AT151225T
公开(公告)日:1997-04-15
申请号:AT94905690
申请日:1994-01-24
Applicant: BASF AG
Inventor: BUSCHMANN ERNST , KLEIN ULRICH , NEUMANN ULRICH , RENZ GUENTER
IPC: A01N37/02 , C07C69/145
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公开(公告)号:AU6221096A
公开(公告)日:1997-01-09
申请号:AU6221096
申请日:1996-06-03
Applicant: BASF AG
Inventor: DEKRAMER JACOBUS JAN , NEUMANN ULRICH , KLEIN ULRICH , MEIWALD MECHTILD , KRIEG WOLFGANG
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公开(公告)号:HUT71917A
公开(公告)日:1996-02-28
申请号:HU9501904
申请日:1993-12-17
Applicant: BASF AG
Inventor: GOETZ NORBERT , HARREUS ALBRECHT , MAYWALD VOLKER , KLEIN ULRICH , MISSLITZ ULF , RANG HARALD
IPC: C07C239/20 , C07C251/54 , C07C253/30 , C07C255/54 , C07C259/06
Abstract: PCT No. PCT/EP93/03597 Sec. 371 Date Jun. 6, 1995 Sec. 102(e) Date Jun. 6, 1995 PCT Filed Dec. 17, 1993 PCT Pub. No. WO94/14757 PCT Pub. Date Jul. 7, 1994Hydroxylamine ethers I I (where X is NO2, CN, halogen, alkyl or haloalkyl, Y is H, NO2, CN, halogen, alkyl or haloalkyl, n is 0-2 or 1-4 where Y and all radicals X are halogen and Alk is unsubstituted or substituted alkylene) and their salts with mineral acids or strong organic acids are prepared by reacting either a hydroximino compound II II (where R1 is alkyl, R2 is alkyl or alkoxy or R1+R2 form an alkylene chain) in the presence of an alkali metal hydroxide, alkali metal alcoholate, alkali metal bicarbonate or alkali metal carbonate as the base, or the corresponding anion II directly, with an alkylating agent III III (where R3 is unsubstituted or substituted alkyl or unsubstituted or substituted phenyl) to give an oximino derivative IV IV said derivative is cleaved by means of a mineral acid or a strong organic acid to give the salt of I and, if desired, the latter is converted by means of a base into the free compound I. The hydroxylamine ethers I are intermediates for crop protection agents and drugs.
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