1.
    发明专利
    未知

    公开(公告)号:DE4335497A1

    公开(公告)日:1995-04-20

    申请号:DE4335497

    申请日:1993-10-19

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP94/03331 Sec. 371 Date Mar. 29, 1996 Sec. 102(e) Date Mar. 29, 1996 PCT Filed Oct. 10, 1994 PCT Pub. No. WO95/11237 PCT Pub. Date Apr. 27, 1995A process for preparing asymmetrically substituted triazines of the formula I I where R1 is hydrogen, methyl or ethyl, R2 and R3 independently of one another are an unsubstituted or substituted hydrocarbon radical, by reaction of a cyanoguanidine of the formula II II with a carboxylic acid derivative in the presence of an alcohol of the formula III R2-OHIII,which comprises reacting a carboxylic acid ester of the formula IV R3-COOR4IV,where R3 has the abovementioned meaning and R4 is an unsubstituted or substituted hydrocarbon radical, in the presence of a base or of a carboxamide selected from the group consisting of N,N-dialkylformamide, N,N-dialkylacetamide and N-methylpyrrolidone and in the presence of a salt or of a salt-like compound of the elements magnesium, calcium, aluminum, zinc, copper, iron, cobalt, nickel or chromium, is described.

    3.
    发明专利
    未知

    公开(公告)号:DE19723473A1

    公开(公告)日:1998-12-10

    申请号:DE19723473

    申请日:1997-06-04

    Applicant: BASF AG

    Abstract: The invention relates to a method for producing chiral 3,4-dehydroprolines of formula (I), in which R, R' and R'' have the meanings given in the description. The invention is characterized in that a pyrrolecarboxylic acid derivative of formula (II) is reacted first with an alkali or alkaline earth metal in ammonia and then with an aqueous salt solution or a compound having formula (III), in which X is a leaving group.

    4.
    发明专利
    未知

    公开(公告)号:DE3904082A1

    公开(公告)日:1990-08-16

    申请号:DE3904082

    申请日:1989-02-11

    Applicant: BASF AG

    Abstract: Process for the preparation of N-substituted 3,4,5,6- tetrahydrophthalimides of the formula I in which R represents hydrogen or fluorine R is hydrogen, chlorine, bromine or a C1- to C4-alkyl group and in which R represents a C1- to C6-alkyl or a C5- to C6-cycloalkyl group, by reacting an aldehyde of the formula II with a phosphorane of the formula III in which Ar represents an unsubstituted or substituted phenyl radical, at temperatures from -10 DEG C to 100 DEG C and in the presence of a solvent.

    7.
    发明专利
    未知

    公开(公告)号:DK0421225T3

    公开(公告)日:1995-06-19

    申请号:DK90118275

    申请日:1990-09-24

    Applicant: BASF AG

    Abstract: Preparation of alpha -chloro-phosphorylidene of the formula I … … in which …… the radicals Ar represent identical or different aryl groups and … E represents an ylide (I)-stabilising substituent, … by reaction of a phosphonium salt of the general formula II … … in which… Hal is chlorine, bromine or iodine,… with a chlorinating agent, using chlorinated lime as the chlorinating agent.

    8.
    发明专利
    未知

    公开(公告)号:AT120752T

    公开(公告)日:1995-04-15

    申请号:AT90118275

    申请日:1990-09-24

    Applicant: BASF AG

    Abstract: Preparation of alpha -chloro-phosphorylidene of the formula I … … in which …… the radicals Ar represent identical or different aryl groups and … E represents an ylide (I)-stabilising substituent, … by reaction of a phosphonium salt of the general formula II … … in which… Hal is chlorine, bromine or iodine,… with a chlorinating agent, using chlorinated lime as the chlorinating agent.

    9.
    发明专利
    未知

    公开(公告)号:DE4037840A1

    公开(公告)日:1992-06-11

    申请号:DE4037840

    申请日:1990-11-28

    Applicant: BASF AG

    Abstract: The invention concerns the preparation of 3-(3,4,5,6-tetrahydrophthalimido)cinnamic acid esters of formula (I) (R = H, halogen; R , R = halogen; R = C-organic rest; R = H, CH3) by the reduction of 3-nitrocinnamic acid esters of formula (II) with hydrogen in the presence of a catalyst and the condensation of the 3-aminocinnamic acid esters obtained of formula (III) with a 3,4,5,6-tetrahydrophthalic acid anhydride of formula (IV). 3-(3,4,5,6-tetrahydrophthalimido)cinnamic acid esters of formula (I) are useful active agents in the plant-protection field.

    Prepn. of olefinic cpds. - by reaction of ylid or phosphonium salt with ketone in 1-6c alcohol to give e.g. herbicides

    公开(公告)号:DE3941562A1

    公开(公告)日:1991-06-20

    申请号:DE3941562

    申请日:1989-12-16

    Applicant: BASF AG

    Abstract: Prepn. of olefinic cpds. of formula (I) comprises: (a) reaction of a phosphonium salt of formula (V) dissolved n a 1-6C alcohol, with a base and elemental bromine to give a Br-contg. phsophonium slat of formula (III) or a Br-contg. phsophorous of formula (IV); and (b) reaction of a ketone of formula (II) with (III) and a base or with (IV), in a solvent. R1 = an organic gp; R2 = an orgnaic gp. or H; A = COR3, COOR3, CONR3R4 or CN; R3, R4 = an organic gp; X = an anion of a strong acid. The prepn. of (IV) in a 1-6C alcohol is claimed per use. USE/ADVANTAGE - Some +-bromo-substd. cinnamic acid derivs. or vinyl ketones prepd. by this process, e.g. N-(3-(methyl-+-bromo acrylate)-4-chlorophenyl) -3,4,5,6-tetrahydronaphthalimide (Ia) are herbicidally active or are intermediates in herbicide prepn. Previous prepns. of (III) and (IV) took place in solvents, e.g. C6H6, CH3COOH, which are unsuited to Wittig-style reactions or are toxic.

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