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公开(公告)号:ES2091278T3
公开(公告)日:1996-11-01
申请号:ES91121148
申请日:1991-12-10
Applicant: BASF AG
Inventor: WINGERT HORST DR , WOLF BERND DR , BENOIT REMY DR , SAUTER HUBERT DR , HEPP MICHAEL DR , GRAMMENOS WASSILIOS DR
IPC: C07C69/736 , C07C20060101 , C07C51/09 , C07C51/367 , C07C59/68 , C07C65/21 , C07C65/24 , C07C67/22 , C07C69/738 , C07C69/76 , C07C235/34 , C07C235/78 , C07C249/08 , C07C251/48 , C07C253/14 , C07C255/17 , C07C255/40 , C07C317/24
Abstract: Prepn. of 2-phenoxymethyl benzoic acid derivs. of formula (I) comprises (a) converting a phenol of formula (II) to the phenolate in the presence of a basic diluent; (b) mixing the mixt. with a lactone of formula (III); (c) distilling off the diluent; (d) reacting the mixt. at 50-250 degrees C in the melt; and (e) dissolving the liq. melt with water and acidifying. X, Y = halogen, 1-4C alkyl, 1-4C alkoxy or CF3; m = 0-4; n = 0-3.
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公开(公告)号:CZ281007B6
公开(公告)日:1996-05-15
申请号:CS47590
申请日:1990-02-01
Applicant: BASF AG
Inventor: SCHUETZ FRANZ DR , SAUTER HUBERT DR , HARREUS ALBRECHT DR , ROHR WOLFGANG DR , HEPP MICHAEL DR , BRAND SIEGBERT DR , WENDEROTH BERND DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N37/10 , A01N37/50 , A01N37/52 , C07C251/38 , C07C251/48 , C07C251/50 , C07C251/52 , C07C251/54 , C07C251/60 , C07C255/62
Abstract: Substituted oxime ethers of the general formula where R1 is alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, alkoxyalkyl, cycloalkyl, cycloalkylalkyl, cyanoalkyl, alkoxycarbonylalkyl, arylalkyl, heteroarylalkyl, arylalkenyl or aryloxyalkyl, the aromatic or heteroaromatic ring being substituted or unsubstituted, R2 and R3 are hydrogen, alkyl, haloalkyl, alkoxy, haloalkoxy, halogen, cyano or nitro, R4 is hydrogen, alkyl or aryl, the aromatic ring being substituted or unsubstituted, and X is CH or N, and fungicides containing these compounds.
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公开(公告)号:DE3917352A1
公开(公告)日:1990-11-29
申请号:DE3917352
申请日:1989-05-27
Applicant: BASF AG
Inventor: WENDEROTH BERND DR , SAUTER HUBERT DR , WINGERT HORST DR , HEPP MICHAEL DR , BRAND SIEGBERT DR , KUEKENHOEHNER THOMAS DR , ROEHL FRANZ DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: C07C69/734 , A01N37/46 , A01N37/50 , C07C45/44 , C07C47/575 , C07C69/736 , C07C69/738 , C07C205/37 , C07C251/48 , C07C255/37 , C07C255/54
Abstract: Oxime ethers of the formula I where X (m=1 to 5) denotes identical or different substituents selected from halogen, cyano, nitro, alkyl, cycloalkyl, alkenyl, alkoxy, haloalkyl, haloalkoxy, substituted or unsubstituted phenyl, substituted or unsubstituted phenoxy, substituted or unsubstituted benzyl or a substituted or unsubstituted fused aromatic ring, with the exception of several known compounds, and fungicides containing these novel compounds.
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公开(公告)号:DE59108848D1
公开(公告)日:1997-10-09
申请号:DE59108848
申请日:1991-12-10
Applicant: BASF AG
Inventor: WINGERT HORST DR , WOLF BERND DR , BENOIT REMY DR , SAUTER HUBERT DR , HEPP MICHAEL DR , GRAMMENOS WASSILIOS DR , KUEKENHOEHNER THOMAS DR
IPC: C07C69/736 , C07C20060101 , C07C51/09 , C07C51/367 , C07C59/68 , C07C65/21 , C07C65/24 , C07C67/22 , C07C69/738 , C07C69/76 , C07C235/34 , C07C235/78 , C07C249/08 , C07C251/48 , C07C253/14 , C07C255/17 , C07C255/40 , C07C317/24
Abstract: Prepn. of 2-phenoxymethyl benzoic acid derivs. of formula (I) comprises (a) converting a phenol of formula (II) to the phenolate in the presence of a basic diluent; (b) mixing the mixt. with a lactone of formula (III); (c) distilling off the diluent; (d) reacting the mixt. at 50-250 degrees C in the melt; and (e) dissolving the liq. melt with water and acidifying. X, Y = halogen, 1-4C alkyl, 1-4C alkoxy or CF3; m = 0-4; n = 0-3.
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公开(公告)号:AT157643T
公开(公告)日:1997-09-15
申请号:AT96101038
申请日:1991-12-10
Applicant: BASF AG
Inventor: WINGERT HORST DR , WOLF BERND DR , BENOIT REMY DR , SAUTER HUBERT DR , HEPP MICHAEL DR , GRAMMENOS WASSILIOS DR , KUEKENHOEHNER THOMAS DR
IPC: C07C69/736 , C07C20060101 , C07C51/09 , C07C51/367 , C07C59/68 , C07C65/21 , C07C65/24 , C07C67/22 , C07C69/738 , C07C69/76 , C07C235/34 , C07C235/78 , C07C249/08 , C07C251/48 , C07C253/14 , C07C255/17 , C07C255/40 , C07C317/24
Abstract: Prepn. of 2-phenoxymethyl benzoic acid derivs. of formula (I) comprises (a) converting a phenol of formula (II) to the phenolate in the presence of a basic diluent; (b) mixing the mixt. with a lactone of formula (III); (c) distilling off the diluent; (d) reacting the mixt. at 50-250 degrees C in the melt; and (e) dissolving the liq. melt with water and acidifying. X, Y = halogen, 1-4C alkyl, 1-4C alkoxy or CF3; m = 0-4; n = 0-3.
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公开(公告)号:AT157079T
公开(公告)日:1997-09-15
申请号:AT96101025
申请日:1991-12-10
Applicant: BASF AG
Inventor: WINGERT HORST DR , WOLF BERND DR , BENOIT REMY DR , SAUTER HUBERT DR , HEPP MICHAEL DR , GRAMMENOS WASSILIOS DR , KUEKENHOEHNER THOMAS DR
IPC: C07C69/736 , C07C20060101 , C07C51/09 , C07C51/367 , C07C59/68 , C07C65/21 , C07C65/24 , C07C67/22 , C07C69/738 , C07C69/76 , C07C235/34 , C07C235/78 , C07C249/08 , C07C251/48 , C07C253/14 , C07C255/17 , C07C255/40 , C07C317/24
Abstract: Prepn. of 2-phenoxymethyl benzoic acid derivs. of formula (I) comprises (a) converting a phenol of formula (II) to the phenolate in the presence of a basic diluent; (b) mixing the mixt. with a lactone of formula (III); (c) distilling off the diluent; (d) reacting the mixt. at 50-250 degrees C in the melt; and (e) dissolving the liq. melt with water and acidifying. X, Y = halogen, 1-4C alkyl, 1-4C alkoxy or CF3; m = 0-4; n = 0-3.
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公开(公告)号:AT143356T
公开(公告)日:1996-10-15
申请号:AT91121148
申请日:1991-12-10
Applicant: BASF AG
Inventor: WINGERT HORST DR , WOLF BERND DR , BENOIT REMY DR , SAUTER HUBERT DR , HEPP MICHAEL DR , GRAMMENOS WASSILIOS DR , KUEKENHOEHNER THOMAS DR
IPC: C07C69/736 , C07C20060101 , C07C51/09 , C07C51/367 , C07C59/68 , C07C65/21 , C07C65/24 , C07C67/22 , C07C69/738 , C07C69/76 , C07C235/34 , C07C235/78 , C07C249/08 , C07C251/48 , C07C253/14 , C07C255/17 , C07C255/40 , C07C317/24
Abstract: Prepn. of 2-phenoxymethyl benzoic acid derivs. of formula (I) comprises (a) converting a phenol of formula (II) to the phenolate in the presence of a basic diluent; (b) mixing the mixt. with a lactone of formula (III); (c) distilling off the diluent; (d) reacting the mixt. at 50-250 degrees C in the melt; and (e) dissolving the liq. melt with water and acidifying. X, Y = halogen, 1-4C alkyl, 1-4C alkoxy or CF3; m = 0-4; n = 0-3.
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公开(公告)号:ES2077891T3
公开(公告)日:1995-12-01
申请号:ES92102914
申请日:1992-02-21
Applicant: BASF AG
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公开(公告)号:DE4042282A1
公开(公告)日:1992-07-02
申请号:DE4042282
申请日:1990-12-31
Applicant: BASF AG
Inventor: KUEKENHOEHNER THOMAS DR , WINGERT HORST DR , WOLF BERND DR , BENOIT REMY DR , HEPP MICHAEL DR , GRAMMENOS WASSILIOS DR , SAUTER HUBERT DR
IPC: C07C51/367 , C07C65/24 , C07C69/738 , C07C235/34 , C07C249/08 , C07C251/48 , C07C253/14 , C07C255/17 , C07C317/24
Abstract: Prepn. of E-oxime-ethers of phenylglyoxylic acid esters of formula (I) comprises (a) reacting a phenol Xm-Ph-PH in a base in the presence of a solvent to give a phenolate; (b) mixing with a lactone of formula (III); (c) distilling off solvent and reacting the mixt. at 50-250 deg.C in the melt; (d) washing with water and acid to give a 2-phenoxymethylbenzoic acid of formula (IV); Q = OH); (e) treating with phosgene or SOCl2 to give the 2-phenoxymethylbenzoyl chloride (IV; Q = Cl); (f) reacting with alkali(ne earth)metal cyanide opt. in the presence of prussic acid; (g) treating the 2-phenoxymethylbenzoyl cyanide (IV; Q = CN) with MeOH in the presence of acid to give (VIIb); (h) opt. splitting under acidic conditions to give (IV; Q = C(O)NHR) or (i) treating (IV; Q=R) with dimethyl sulphoxide in the presence of a base to give a beta ketosulphoxide (IV; Q = CH2SOCH3) and treating with a halogenating agent, and MeOH in acid to give (IV; Q = C(O)OMe); (k) reacting (IV; Q = C(O)OMe) and/or (VIIb) with O-methylhydroxylamine or its acid addn. salt to give (I). Q = R1CH2SOMe, OH, Cl, CN or C(O)NNR; X, Y = halo, 1-4C alkyl, 1-4C alkoxy or CF3; m = 0-4; n = 0-3; R = 1-4C alkyl.
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公开(公告)号:DE4042280A1
公开(公告)日:1992-07-02
申请号:DE4042280
申请日:1990-12-31
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS DR , WINGERT HORST DR , WOLF BERND DR , KUEKENHOEHNER THOMAS DR , BENOIT REMY DR , HEPP MICHAEL DR , SAUTER HUBERT DR
IPC: C07C51/367 , C07C65/24 , C07C69/738 , C07C235/34 , C07C249/08 , C07C251/48 , C07C253/14 , C07C255/17 , C07C317/24
Abstract: Prepn. of E-oxime-ethers of phenylglyoxylic acid esters of formula (I) comprises (a) reacting a phenol Xm-Ph-PH in a base in the presence of a solvent to give a phenolate; (b) mixing with a lactone of formula (III); (c) distilling off solvent and reacting the mixt. at 50-250 deg.C in the melt; (d) washing with water and acid to give a 2-phenoxymethylbenzoic acid of formula (IV); Q = OH); (e) treating with phosgene or SOCl2 to give the 2-phenoxymethylbenzoyl chloride (IV; Q = Cl); (f) reacting with alkali(ne earth)metal cyanide opt. in the presence of prussic acid; (g) treating the 2-phenoxymethylbenzoyl cyanide (IV; Q = CN) with MeOH in the presence of acid to give (VIIb); (h) opt. splitting under acidic conditions to give (IV; Q = C(O)NHR) or (i) treating (IV; Q=R) with dimethyl sulphoxide in the presence of a base to give a beta ketosulphoxide (IV; Q = CH2SOCH3) and treating with a halogenating agent, and MeOH in acid to give (IV; Q = C(O)OMe); (k) reacting (IV; Q = C(O)OMe) and/or (VIIb) with O-methylhydroxylamine or its acid addn. salt to give (I). Q = R1CH2SOMe, OH, Cl, CN or C(O)NNR; X, Y = halo, 1-4C alkyl, 1-4C alkoxy or CF3; m = 0-4; n = 0-3; R = 1-4C alkyl.
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