公开(公告)号：FI972193A0

公开(公告)日：1997-05-22

申请号：FI972193

申请日：1997-05-22

Applicant: BASF AG

Inventor： ISAK HEINZ ,  KEIL MICHAEL ,  WOLF BERND ,  WINGERT HORST ,  WETTLING THOMAS

IPC: C07B61/00 ,  C07C253/14 ,  C07C255/40 ,  C07C

Abstract: PCT No. PCT/EP95/04463 Sec. 371 Date May 6, 1997 Sec. 102(e) Date May 6, 1997 PCT Filed Nov. 14, 1995 PCT Pub. No. WO96/16023 PCT Pub. Date May 30, 1996Halomethylbenzoyl cyanides I PH-CO-CN (I) where Ph is phenyl which is substituted by chloromethyl or bromomethyl and may cary 1-4 other rradicals, are prepared from halomethylbenzoyl chlorides II PH-CO-Cl (II), by reacting II with a cyanide-donating compound in the presence of a Lewis acid, if required in an inert organic solvent or diluent, and then isolating the product. The halomethylbenzoyl cyanides I are important intermediates for synthesizing crop protection agents.

公开(公告)号：HUT66608A

公开(公告)日：1994-12-28

申请号：HU9400996

申请日：1994-04-07

Applicant: BASF AG

Inventor： WETTLING THOMAS ,  WOLF BERND ,  KEIL MICHAEL ,  ISAK HEINZ ,  DOETZER REINHARD

IPC: C07C253/14 ,  C07C255/32 ,  C07C255/40

Abstract: A process for preparing halomethylbenzoyl cyanides I Ph-CO-CNI (Ph=phenyl radical substituted by chloromethyl or bromomethyl which, if desired, can additionally carry 1-4 further radicals) by reacting halomethylbenzoyl chlorides II Ph-CO-ClII with an alkali metal cyanide or transition metal cyanide, if appropriate in an organic diluent, and novel halomethylbenzoyl cyanides I' I' (X=halogen, C1-C4-alkyl, C1-C4-alkoxy, CF3, C1-C5-alkyl-(C1-C5-alkyl)hydroxyimino or C1-C5-alkyl-(C2-C5-alkenyl)hydroxyimino; m=0 to 4 and Y=chloromethyl or bromomethyl) are described. The halomethylbenzoyl cyanides I are important intermediates for the synthesis of plant protection agents.

公开(公告)号：AU641579B2

公开(公告)日：1993-09-23

申请号：AU9008291

申请日：1991-12-24

Applicant: BASF AG

Inventor： WINGERT HORST ,  WOLF BERND ,  BENOIT REMY ,  SAUTER HUBERT ,  HEPP MICHAEL ,  GRAMMENOS WASSILIOS ,  KUEKENHOEHNER THOMAS

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.

公开(公告)号：DE3686573D1

公开(公告)日：1992-10-01

申请号：DE3686573

申请日：1986-12-19

Applicant: BASF AG

Inventor： WOLF BERND ,  THEOBALD HANS ,  BECKER RAINER ,  GOETZ NORBERT ,  HIMMELE WALTER ,  KROPP RUDOLF

IPC: A01N43/08 ,  A01N43/10 ,  A01N53/00 ,  A01N53/04 ,  A01N53/08 ,  C07C249/00 ,  C07D261/04 ,  C07D307/40 ,  C07D307/42 ,  C07D307/45 ,  C07D307/46 ,  C07D307/54 ,  C07D409/12

Abstract: 2-benzylfuryl cpds of formula (I) are new R1, R2 and R3 are each H, halogen, (halo-)alkyl, (halo)alkoxy, haloalkylthio, or (halo)alkenyl, each contg. upto 6C; n is 1,3 if R3 is not H; R4 and R5 are H or 1-6C alkyl; R is CHO or CHR6OA; R6 is H, CN, alkyl, (halo)alkenyl, or alkynyl each contg. up to 6C, or carbonamido; A is H or the gp of an acid typical for pyrethroids; if R2 is not H, Cl, Br, Me or MeO if at the same time R1 isH or Me, R3 is H and A is H; if R1 and R2 are not Me if A is the gp of tetramethylcyclopropanoic acid; and if R2 is not Me, Cl, Br or MeO and R1 and R3 are not H if A is the gp of chrysanthemumic acid.

公开(公告)号：AU2346488A

公开(公告)日：1989-04-13

申请号：AU2346488

申请日：1988-10-06

Applicant: BASF AG

Inventor： SCHUETZ FRANZ ,  SAUTER HUBERT ,  SCHIRMER ULRICH ,  WOLF BERND ,  AMMERMANN EBERHARD ,  POMMER ERNST-HEINRICH

IPC: C07C331/14 ,  A01N35/08 ,  A01N37/00 ,  A01N37/02 ,  A01N37/06 ,  A01N37/18 ,  A01N37/34 ,  A01N37/36 ,  A01N37/38 ,  A01N37/40 ,  A01N37/44 ,  A01N37/48 ,  A01N39/02 ,  A01N43/04 ,  A01N43/08 ,  A01N43/36 ,  A01N45/00 ,  A01N47/48 ,  A01N49/00 ,  A01N53/00 ,  A01N53/06 ,  A01N59/24 ,  C07C67/00 ,  C07C67/11 ,  C07C69/007 ,  C07C69/025 ,  C07C69/608 ,  C07C69/612 ,  C07C69/614 ,  C07C69/62 ,  C07C69/73 ,  C07C69/732 ,  C07C69/734 ,  C07C69/74 ,  C07C69/75 ,  C07C69/76 ,  C07C69/78 ,  C07C69/92 ,  C07C201/00 ,  C07C205/56 ,  C07C213/00 ,  C07C219/22 ,  C07C229/12 ,  C07C233/00 ,  C07C233/12 ,  C07C235/34 ,  C07C235/42 ,  C07C237/20 ,  C07C253/00 ,  C07C255/07 ,  C07C255/34 ,  C07C255/38 ,  C07C255/53 ,  C07C313/00 ,  C07C323/16 ,  C07C323/20 ,  C07C323/56 ,  C07C323/62 ,  C07C325/00 ,  C07D207/327 ,  C07D295/155 ,  C07D307/16 ,  C07D307/54 ,  C07D307/68 ,  C07C69/767 ,  C07C69/753 ,  C07C69/743 ,  C07C69/24 ,  C07C121/75 ,  C07C103/26 ,  C07C149/273 ,  A01N37/10 ,  A01N37/08 ,  C07D207/30

Abstract: Ortho-substituted benzyl carboxylates of the formula I where R1 is alkoxy, alkylthio, halogen or amino, R2 is alkoxycarbonyl, cyano or CONH2, R3 l is hydrogen, halogen, cyano, aryl, aryloxy, a saturated or unsaturated heterocyclic radical, cycloalkyl, or substituted cyclopropyl, X is alkylene, and n is 0 or 1, and fungicides containing these compounds.

公开(公告)号：BRPI0610721A2

公开(公告)日：2016-11-16

申请号：BRPI0610721

申请日：2006-04-21

Applicant: BASF AG

Inventor： WOLF BERND ,  BUDICH MANUEL ,  KEIL MICHAEL ,  RACK MICHAEL ,  SMIDT SEBASTIAN PEER ,  MAYWALD VOLKER

IPC: C07C17/12 ,  C07C17/20 ,  C07C17/23 ,  C07C25/13

公开(公告)号：AU2005266622B8

公开(公告)日：2011-05-19

申请号：AU2005266622

申请日：2005-07-13

Applicant: BASF AG

Inventor： LOEHR SANDRA ,  SCHMIDT THOMAS ,  MAYER GUIDO ,  GEBHARDT JOACHIM ,  KEIL MICHAEL ,  WOLF BERND

IPC: C07D239/54 ,  C07C307/06

Abstract: The present invention relates to a process for preparing 3-phenyl(thio)uracils and -dithiouracils of the formula I where the variables are each as defined in the description, and also intermediates for their preparation.

公开(公告)号：PL205226B1

公开(公告)日：2010-03-31

申请号：PL37105703

申请日：2003-02-06

Applicant: BASF AG

Inventor： MAYER GUIDO ,  CULLMANN OLIVER ,  WOLF BERND ,  KEIL MICHAEL

IPC: C07C249/12 ,  C07B61/00 ,  C07C251/38 ,  C07C251/48

公开(公告)号：PE20081460A1

公开(公告)日：2008-12-07

申请号：PE2007001378

申请日：2007-10-12

Applicant: BASF AG

Inventor： SCHMIDT THOMAS ,  GEBHARDT JOACHIM ,  LOHR SANDRA ,  KEIL MICHAEL ,  WEVERS JAN HENDRIK ,  ERK PETER ,  SAXELL HEIDI EMILIA ,  HAMPRECHT GERHARD ,  SEITZ WERNER ,  MAYER GUIDO ,  WOLF BERND ,  COX GERHARD ,  MICHEL ALFRED ,  ZAGAR CYRILL ,  REINHARD ROBERT ,  SIEVERNICH BERND

IPC: A01N43/48 ,  A01N43/54 ,  C07D239/54

Abstract: SE REFIERE A UNA FORMA CRISTALINA II DE 2-CLORO-5-[3,6-DIHIDRO-3-METIL-2,6-DIOXO-4-(TRIFLUOROMETIL)-1-(2H)-PIRIMIDINIL]-4-FLUORO-N-[[METIL(1-METILETIL)AMINO]SULFONIL]BENZAMIDA O FENILURACILO I, EXCENTA DE SOLVENTE, QUE PRESENTA UN DIAFRACTOGRAMA DE RAYOS X QUE MUESTRAN AL MENOS DOS DE LOS SIGUIENTES REFLEJOS EXPRESADOS EN 2 THETA: 6,3; 9,4; 10,9; 11,9; 12,6; 15,0; 15,8; 17,1 ± 0,3; ENTRE OTROS; Y UN PICO DE FUSION DENTRO DEL RANGO QUE VA DE 170 A 200 ºC. TAMBIEN SE REFIERE A UNA COMPOSICION FITOPROTECTORA PREFERENTEMENTE EN FORMA DE CONCENTRADO DE SUSPENSION ACUOSO O NO ACUOSO; Y UN PROCEDIMIENTO DE PREPARACION, SIENDO UTIL PARA CONTROLAR EL CRECIMIENTO DE VEGETACION NO DESEADA

公开(公告)号：DE502004005772D1

公开(公告)日：2008-01-31

申请号：DE502004005772

申请日：2004-12-01

Applicant: BASF AG

Inventor： HAMPRECHT GERHARD ,  PUHL MICHAEL ,  WOLF BERND ,  KEIL MICHAEL ,  REINHARD ROBERT ,  SEITZ WERNER ,  MAYER GUIDO

IPC: C07D239/56 ,  C07D239/54

Abstract: A process is described for preparing 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I, by reacting a phenyl iso(thio)cyanate of the formula II with an enamine of the formula III and, if appropriate, in a further step, the resulting 3-phenyl(thio)uracil or 3-phenyldithiouracil of the formula I where R1=R1a, when R1=hydrogen, is reacted with an aminating agent of the formula IV to give 3-phenyl(thio)uracils or 3-phenyldithiouracils of the formula I where R1=amino where the variables R1, R1a, R2, R3, R4, X1, X2, X3, Ar, A and L1 are each as defined in claim 1.