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公开(公告)号:DE4441673A1
公开(公告)日:1996-05-30
申请号:DE4441673
申请日:1994-11-23
Applicant: BASF AG
Inventor: MUELLER BERND DR , GRAMMENOS WASSILIOS DR , SAUTER HUBERT DR , ROEHL FRANZ DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , GOETZ NORBERT DR
IPC: C07C259/06 , A01N37/22 , A01N37/34 , A01N47/24 , C07C271/12 , C07C271/28 , C07C271/38 , C07C271/60 , C07C275/32 , C07C269/00 , C07C273/02 , C07C205/31 , C07C217/76 , C07D213/26 , C07D213/36 , A01N43/40 , A01N47/10
Abstract: 2-[4-biphenyl-oxymethylene]-anilides have the formula (I), in which the indices and substituents have the following meanings: R, R , R stand for cyano, nitro, halogen, alkyl, alkyl halide, alkoxy, alkoxy halide, alkylthio, alkylthio halide, alkylamino, dialkylamino, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, di-alkylaminocarbonyl, alkylcarbonylamino, alkylcarbonyl-(alkylamino), alkenyl, alkenyloxy, alkinyl, alkinyloxy, cycloalkyl or C(R )=NOR ; R , R stand for hydrogen, alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl; m equals 1, 2, 3, 4 or 5; n equals 0, 1 or 2; R equals nitro, cyano, halogen, optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy, alkinyloxy or alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylcarbonylamino, alkylcarbonyl-(alkylamino) or C(R )=NOR ; o equals 0, 1, 2, 3 or 4; R stands for hydrogen, optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, alkylcarbonyl or alkoxycarbonyl; X stands for a direct bond or CH2, O or NR ; R stands for hydrogen, alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl; R stands for alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl and when X stands for NR it may also stand for hydrogen. Also disclosed are a process and intermediate products for preparing the same and their use.
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公开(公告)号:DE4312637A1
公开(公告)日:1994-10-20
申请号:DE4312637
申请日:1993-04-19
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS DR , SIEGEL WOLFGANG DR , OBERDORF KLAUS DR , MUELLER BERND DR , SAUTER HUBERT DR , DOETZER REINHARD DR
IPC: C07B61/00 , C07C45/46 , C07C45/48 , C07C49/84 , C07C65/40 , C07C67/313 , C07C69/734 , C07C69/736 , C07C235/34 , C07C235/80 , C07C251/48 , C07C255/54 , C07D213/50 , C07C255/49 , C07C45/00 , C07C49/175 , C07C59/68 , C07C65/21 , C07C327/22 , A01N37/50 , A01N37/36 , A01N43/40
Abstract: The process is characterised in that 4-alkanoylaryl benzyl ethers of the general formula I where the variables have the following meaning: R is hydrogen, halogen, cyano; alkyl, alkoxy; X is CH2, CH-CH3, CH-CH2-CH3, CH-OCH3, N-OCH3; Y is oxygen, sulphur, a direct bond or nitrogen; m is 0, 1, 2 or 3; R is hydrogen; alkyl, alkenyl, alkynyl, alkoxy; R is cyano, halogen, alkyl, alkoxy, haloalkyl; R is alkyl, haloalkyl; cycloalkyl; or an optionally substituted mono- to trinuclear aromatic system, are prepared by reacting an aryl benzyl ether of the general formula II where X, Y, R, R , R and m have the abovementioned meaning, with a carboxylic acid halide or with a carboxylic anhydride or with a carboxylic - sulphonic anhydride in the presence of an acid and optionally in the presence of a diluent.
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123.
公开(公告)号:CZ140193A3
公开(公告)日:1994-10-19
申请号:CZ140193
申请日:1993-07-14
Applicant: BASF AG
Inventor: OBERDORF KLAUS DR , SAUTER HUBER DR , GRAMMENOS WASSILIOS DR , KIRSTGEN REINHARD DR , HARRIES VOLKER DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR , GOLD RANDALL EVAN DR , SIEGEL WOLFGANG DR , HARREUS ALBRECHT DR
IPC: A01N37/18 , A01N37/34 , A01N37/36 , A01N37/38 , A01N37/50 , C07C251/40 , C07C251/48 , C07C251/50 , C07C251/52 , C07C251/54 , C07C251/58 , C07C251/60 , C07C255/32 , C07C255/62 , C07D213/63 , C07D333/32 , C07D521/00
Abstract: Substituted oxime ethers of the general formula I in which R denotes alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, alkoxyalkyl, cycloalkyl, cycloalkylalkyl, cyanoalkyl, alkoxycarbonylalkyl, arylalkyl, heteroarylalkyl, arylalkenyl or aryloxyalkyl, the aromatic or heteroaromatic ring optionally being substituted, R and R denote hydrogen, alkyl, haloalkyl, alkoxy, haloalkoxy, halogen, cyano or nitro, R denotes hydrogen, alkyl, cycloalkyl, haloalkyl or aryl, the aromatic ring optionally being substituted and R and R are identical or different and denote hydrogen or alkyl, and X denotes CH or N, and fungicides and pesticides containing these compounds.
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124.
公开(公告)号:CS43792A3
公开(公告)日:1992-09-16
申请号:CS43792
申请日:1992-02-13
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS DR , HARREUS ALBRECHT DR , SAUTER HUBERT DR , HELLENDAHL BEATE DR , DOETZER REINHARD DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N37/50 , A01N43/54 , A01N43/58 , A01N43/76 , A01N43/836 , C07C69/65 , C07C69/653 , C07C69/734 , C07C69/738 , C07C251/48 , C07C251/50 , C07C251/52 , C07C251/54 , C07C251/56 , C07C251/58 , C07C251/60 , C07C251/86 , C07C255/15 , C07C255/57 , C07C255/58 , C07C255/62 , C07D213/77 , C07D239/42 , C07D241/20 , C07D263/32 , C07D333/28 , C07C251/32 , C07C249/16 , C07C69/73
Abstract: Iminoalkyl-phenylacrylic acid derivs. (I) ar new: R = H or 1-6C alkyl; R = H; 1-4C alkyl opt. substd. by halo; or opt. substd. aryl; Z ,Z = H; halo; CN; NO2;etc.;Y = O; NH; or NR ; and R = H; 1-4C alkoxycarbonyl-1-4C alkyl; or opt. substd. alkyl, cycloalkyl, etc.; or Y+R form a ring which is opt. substd. when Y = NH or NR ; R = 1-6C alkyl; X = CH-1-4C alkoxy or CH-1-4C alkylthio (also 1-4C alkylidene and 1-4C alkoxyimino in the description).
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公开(公告)号:DE4042272A1
公开(公告)日:1992-07-02
申请号:DE4042272
申请日:1990-12-31
Applicant: BASF AG
Inventor: WOLF BERND DR , BENOIT REMY DR , SAUTER HUBERT DR , GRAMMENOS WASSILIOS DR , WINGERT HORST DR , KUEKENHOEHNER THOMAS DR , HEPP MICHAEL 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:DE4042271A1
公开(公告)日:1992-07-02
申请号:DE4042271
申请日:1990-12-31
Applicant: BASF AG
Inventor: BENOIT REMY DR , WINGERT HORST DR , WOLF BERND DR , SAUTER HUBERT DR , KUEKENHOEHNER THOMAS DR , GRAMMENOS WASSILIOS DR , HEPP MICHAEL 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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