METHOD FOR THE PRODUCTION OF ALKOXYCARBONYLAMINO TRIAZINES
    1.
    发明申请
    METHOD FOR THE PRODUCTION OF ALKOXYCARBONYLAMINO TRIAZINES 审中-公开
    用于生产alkoxycarbonylaminotriazines

    公开(公告)号:WO2004054990A3

    公开(公告)日:2005-04-07

    申请号:PCT/EP0314274

    申请日:2003-12-16

    CPC classification number: C07D251/54 C07D251/70

    Abstract: Disclosed is a method for producing alkoxycarbonylamino triazines of formula (I) by reacting diaminotriazines or triaminotriazines with cyclic carbonic acid esters and optional subordinate quantities of acyclic carbonic acid esters in the presence of an alcohol and an alkaline alkanol or alkaline-earth alkanol as a base. In said formula, Y represents hydrogen, C1-C4 alkyl, phenyl that is optionally substituted by C1-C4 alkyl, C1-C4 alkoxy, or halogen, or a radical of formula NR R while R , R , R , R , R , and R independently represent hydrogen or a radical of formula COOX or X, wherein X represents C1-C13 alkyl, the carbon skeleton of which can be interrupted by 1 or 2 oxygen atoms having the function of ether and/or substituted by hydroxy, or C3-C6 alkenyl provided that at least one of the radicals R to R in formula (I) represents COOX, or at least one of the radicals R to R in said formula represents COOX if Y represents NR R .

    Abstract translation: 一种用于由二 - 或与环状碳酸酯triaminotriazines,以及任选的反应在碱金属或碱土金属醇盐作为碱的醇的存在下和无环碳酸酯,少量的生产式(I)的烷氧基​​羰基三嗪处理。 Y'>是氢,C1-C4烷基,任选被C1-C4烷基,C1-C4烷氧基或卤素或下式基团NR <5> - [R <6>和R <1>,R <取代 2>,R <3>,R <4>,R <5>和R <6>各自独立为氢或下式基团COOX或X,其中X是C1-C13烷基,其碳骨架被1或2的 可以是在醚官能氧原子和/或羟基取代,或C 3 -C 6 - 链烯基,表示,其条件是在式(I)R <1>至R <4>,或者当Y中的至少一个 <1> [R <6> <5>是NR,R <1>至R <6> COOX中的至少一个。

    4.
    发明专利
    未知

    公开(公告)号:DE59007079D1

    公开(公告)日:1994-10-13

    申请号:DE59007079

    申请日:1990-05-30

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP90/00866 Sec. 371 Date Nov. 12, 1991 Sec. 102(e) Date Nov. 12, 1991 PCT Filed May 30, 1990 PCT Pub. No. WO90/15087 PCT Pub. Date Dec. 13, 1990.Novel (meth)acrylate copolymers which contain, as polymerized units, A) one or more (meth)acrylates and/or (meth)acrylamides having second order nonlinear optical properties and of the general formula I (I) where R is hydrogen or methyl, X is a flexible spacer, which may or may not be present, Y is a divalent group having electron donor activity and Z is a noncentrosymmetric radical containing an easily polarizable conjugated pi -electron system and one or more electron acceptor groups, and B) one or more (meth)acrylates of alkanols where the alkyl radical is of 10 to 30 carbon atoms in a molar ratio of (A) to (B) of from 1:0.5 to 1:5 are very suitable as nonlinear optical materials for nonlinear optical arrangements and for the production of Langmuir-Blodgett films. The novel (meth)acrylate copolymers which contain terminal nitro, trifluoromethyl, cyano or fulven-6-yl groups as electron acceptors and have molar ratios A to B differing from those mentioned above are also suitable for intended uses outside nonlinear optics.

    (METH)ACRYLATE COPOLYMERIZATES AND THEIR USE IN NON-LINEAR OPTICS AND IN THE PRODUCTION OF LANGMUIR-BLODGETT COATINGS

    公开(公告)号:AU5736690A

    公开(公告)日:1991-01-07

    申请号:AU5736690

    申请日:1990-05-30

    Applicant: BASF AG

    Abstract: PCT No. PCT/EP90/00866 Sec. 371 Date Nov. 12, 1991 Sec. 102(e) Date Nov. 12, 1991 PCT Filed May 30, 1990 PCT Pub. No. WO90/15087 PCT Pub. Date Dec. 13, 1990.Novel (meth)acrylate copolymers which contain, as polymerized units, A) one or more (meth)acrylates and/or (meth)acrylamides having second order nonlinear optical properties and of the general formula I (I) where R is hydrogen or methyl, X is a flexible spacer, which may or may not be present, Y is a divalent group having electron donor activity and Z is a noncentrosymmetric radical containing an easily polarizable conjugated pi -electron system and one or more electron acceptor groups, and B) one or more (meth)acrylates of alkanols where the alkyl radical is of 10 to 30 carbon atoms in a molar ratio of (A) to (B) of from 1:0.5 to 1:5 are very suitable as nonlinear optical materials for nonlinear optical arrangements and for the production of Langmuir-Blodgett films. The novel (meth)acrylate copolymers which contain terminal nitro, trifluoromethyl, cyano or fulven-6-yl groups as electron acceptors and have molar ratios A to B differing from those mentioned above are also suitable for intended uses outside nonlinear optics.

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