New diarylphenoxy-aluminum compound, obtained by a reaction of bis(diarylphenol) ligand with aluminum compound and/or aluminum compound, useful as a catalyst

    公开(公告)号:DE102005044518A1

    公开(公告)日:2007-03-22

    申请号:DE102005044518

    申请日:2005-09-16

    Applicant: BASF AG

    Abstract: Diarylphenoxy-aluminum compound (A), obtained by a reaction of bis(diarylphenol) ligand (I) with aluminum compound (II) and/or aluminum compound (III), is new. Diarylphenoxy-aluminum compound, obtained by a reaction of bis(diarylphenol) ligand of formula (I) with aluminum compound (II) of formula ((R 14>) 3-pAlH p) and/or aluminum compound (III) of formula (MAlH 4), is new. T : 1-6C-alkyl, 1-6C-perfluoroalkyl, 1-6C-alkoxy, 7-12C-aralkyl, halo, optionally substituted 6-10C-aryl or NO 2; Ar 1>-Ar 4>6-15C aryl or 2-15C heteroaryl (optionally substituted by 1-7 substitutions of T, SiR 5>aR 6>aR 7>a, NR 8>aR 9>a or SR 1>0a); either R 1>-R 4>H, T, SiR 5>bR 6>bR 7>b, NR 8>bR 9>b or SR 1>0b; or A+R 1>-R4 : aromatic or non-aromatic cycle; D : O, S, NR 11>, C(O), S(O) and/or S(O) 2; A : 1-25C-hydrocarbon, heteroatom of D, T, 1-10C-acyloxy, SiR 5>cR 6>cR 7>c, 2-10C-heteroaryl, NR 8>cR 9>c, SR 1>0c, 1-12-acyl, 1-10C-carboxyl, 6-15C-aryl or 2-15C-hereroaryl optionally substituted by 1-5 substitutions of T, SiR 5>dR 6>dR 7>d, NR 8>dR 9>d, SR 10>d, heteroatom of D, P(R 11>), (R 11>)P(O) or Si(R 12>R 13>); R 5>a-R 5>d, R 6>a-R 6>d, R 7>a-R 7>d, R 10>a-R 10>d, R 11>-R 13>, R 11>a : 1-6C-alkyl, 7-12C-aralkyl and/or optionally substituted 6-10C-aryl; either R 8>a-R 8>d, R 9>a-R 9>d : 1-6C-alkyl, 7-12C-aralkyl and/or optionally substituted 6-10C-aryl; or R 8>aR 9>a, R 8>bR 9>b, R 8>cR 9>c, R 8>dR 9>d : 2-8C cyclic hydrocarbon containing one or more hetero atoms of O, S or NR 11>a; Al : aluminum; R 14>1-5C-alkyl; p : 0-3; and M : Li, Na or K. Independent claims are included for: (1) a preparation of isopulegol (IV) comprising cyclization of citronellal (V) in the presence of (I) as a catalyst; and (2) a method for preparing menthol comprising preparing (IV) and subsequently hydrogenating the ethylenic double bonds in (IV). [Image].

    METHOD FOR PRODUCING 1-SUBSTITUTED 5- OR 3-HYDROXYPYRAZOLES

    公开(公告)号:BG65026B1

    公开(公告)日:2006-12-29

    申请号:BG10553801

    申请日:2001-05-22

    Applicant: BASF AG

    Abstract: The invention relates to a method for producing 1-substituted 5- and/or 3-hydroxypyrazoles of formula wherein R1 represents C1-C6-alkyl,C2-C6-alkenyl, C2-C6-alkinyl, C3-C6-cycloalkyl or C1-C4-alkoxy, whereby these groups can be substituted by halogen, C1-C4-alkoxy, phenoxy, C1-C6-alkoxycarbonyl, or a cyclic ring system with 3-14 ring atoms, by reacting a 3-alkoxyacrylic acid alkyl ester for formula wherein R2, R3 independently means C1-C6-alkyl or C3-C6 cycloalkyl, with a hydrazine or formula wherein R1 has the above cited meaning, a) at a pH value of 6-11 to form 5-hydroxypyrazoles of formula or b) at a pH value of 11-14 to form 3-hydroxypyrazoles of formula (II).

    Bifunctional phenyliso(thio)cyanates; method and intermediate products for the production thereof

    公开(公告)号:ZA200504331B

    公开(公告)日:2006-07-26

    申请号:ZA200504331

    申请日:2005-05-27

    Applicant: BASF AG

    Abstract: Bifunctional phenyl iso(thio)cyanate derivatives (I) are new. Also new are aniline and nitrobenzene derivative intermediates (II) and (V). Bifunctional phenyl iso(thio)cyanate derivatives of formula W=C=N-Ar-CO-NH-SO 2-A (I) are new. W : O or S; Ar : phenylene (optionally substituted by one or more of halo, 1-4C haloalkyl and CN), and A : NH 2 or the residue of a primary or secondary amine. Independent claims are also included for: (a) preparation of (I); (b) new aniline and nitrobenzene derivative intermediates of formulae H 2N-Ar-CO-NH-SO 2-A (II) and O 2N-Ar-CO-NH-SO 2-A (V), and (c) preparation of 4-(sulfamidocarbonyl-phenyl)-1,2,4-triazolinedione derivatives of formula (VI) by reacting an ester of diaza-ester of formula R 4>-NH-NR 3>-C(W')OR' (VII) and cyclizing the obtained urea derivative of formula R'O-C(=W')-N(R 3>)-N(R 4>)-C(=W)-NH-Ar-CO-NH-SO 2-A (VIII). [Image] W' : O or S; R 3>, R 4> : H, CN, NH 2, 1-6C alkyl, 1-6C haloalkyl, 1-6C alkoxy, 1-6C haloalkoxy, 3-7C cycloalkyl, 2-6C alkenyl, 2-6C haloalkenyl, 3-6C alkynyl, benzyl, OR 5> or (1-3C) cyanoalkyl, or R 3> + R 4> : a group completing 4-7 membered heterocyclyl optionally interrupted by S, O, NR 6> or N and optionally substituted by one or more of halo or 1-4C alkyl; R 5> : H, 1-6C alkyl, 1-6C haloalkyl, 3-7C cycloalkyl, 2-6C alkenyl, 3-6C alkynyl, optionally substituted phenyl or optionally substituted benzyl; R 6> : H, 1-6C alkyl, 3-6C alkenyl or 3-6C alkynyl, and R' : 1-4C alkyl. ACTIVITY : Herbicide. MECHANISM OF ACTION : None given.

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