Optically active phenoxypropionic esters
    1.
    发明授权
    Optically active phenoxypropionic esters 失效
    光学活性苯氧基丙酸酯

    公开(公告)号:US5350873A

    公开(公告)日:1994-09-27

    申请号:US928568

    申请日:1992-08-13

    摘要: Optically active compounds of the formula I ##STR1## where R is C.sub.1 -C.sub.12 -alkyl or -perfluoroalkyl in which one or two non-adjacent CH.sub.2 or CF.sub.2 groups can also be replaced by --O-- and/or --CO-- and/or --CO--O-- and/or --CH.dbd.CH-- and/or --CH-halogen-- and/or --CHCN-- and/or --0--CO--CH-halogen-- and/or --O--CO--CHCN--, or is C.sub.1 -C.sub.12 -alkyl which can have a terminal chemically reactive group and in which a CH.sub.2 group can be replaced by --O--,A.sup.1 and A.sup.2 are each, independently of one another, 1,4-phenylene which is unsubstituted or substituted by one or two F and/or Cl and/or Br atoms and/or CH.sub.3 groups and/or CN groups and in which one or two CH groups can also be replaced by N, 1,4-cyclohexylene in which one or two non-adjacent CH.sub.2 groups can also be replaced by --O-- and/or --S--, 1,4-piperidinediyl, 1,4-bicyclo[2.2.2]octylene, 2,6-naphthalenediyl, decahydro-2,6-naphthalenediyl or 1,2,3,4-tetrahydro-2,6-naphthalenediyl,A.sup.3 is unsubstituted or substituted phenyl,Z is --CO--O--, --O--CO--, --CH.sub.2 CH.sub.2 --, --OCH.sub.2 --, --CH.sub.2 O--, --C.tbd.C-- or a single bond andm is 0, 1, 2 or 3.

    摘要翻译: 其中R是具有一个或两个不相邻的CH2或CF2基团的C1-C12-烷基或全氟烷基的式I的光学活性化合物(I)也可以被-O-和/或-CO- 和/或-CO-O-和/或-CH = CH-和/或-CH-卤素 - 和/或-CHCN-和/或-O-CO-CH-卤素 - 和/或-O-CO- CHCN-或可具有末端化学反应性基团并且其中CH 2基团可被-O-,A 1和A 2取代的C 1 -C 12 - 烷基彼此独立地为彼此独立的1,4-亚苯基,其为 未被取代或被一个或两个F和/或Cl和/或Br原子和/或CH 3基团和/或CN基团取代,并且其中一个或两个CH基团也可被N,1,4-亚环己基代替,其中一个或两个 或两个不相邻的CH 2基团也可以被-O-和/或-S-,1,4-哌啶二基,1,4-二环[2.2.2]亚辛基,2,6-萘二甲酸,十氢-2, 6-萘二基或1,2,3,4-四氢-2,6-萘二基,A3是未取代或取代的苯基,Z是-CO-O-,-O-CO-,-CH2CH2 - , - OCH2 - , - CH2O-,-C3OND C或单键,m为0,1,2或3。

    Monomers and their use for the production of a laser-optical recording
element which can be repeatedly erased and recorded on
    2.
    发明授权
    Monomers and their use for the production of a laser-optical recording element which can be repeatedly erased and recorded on 失效
    单体及其用于生产可以反复擦除并记录的激光光学记录元件

    公开(公告)号:US5187248A

    公开(公告)日:1993-02-16

    申请号:US814516

    申请日:1991-12-30

    IPC分类号: C09K19/38 G11B7/25

    CPC分类号: G11B7/25 C09K19/3857

    摘要: Novel laser-optical recording elements which can be repeatedly erased and recorded on contain recording layers (a) which exhibit enantiotropic, ferroelectric smectic liquid crystalline (S.sub.c*) behavior, so that they can be switched back and forth between two thermodynamically stable, optically distinguishable ferroelectric smectic liquid crystalline S.sub.C* order states on exposure to a laser beam of sufficient luminous power, by applying an external electric field. The recording layers (a) themselves consist mainly or exclusively of novel polymers P having chiral mesogenic side groups. The novel polymers P are prepared using the novel monomers of the general formula I ##STR1## where R is hydrogen, chlorine or methyl, A is a flexible space-maintaining long-chain molecular moiety, and C is an optically active chiral molecular moiety and B is a mesogenic molecular moiety composed of at least three aromatic nuclei which are bonded linearly or virtually linearly to one another, or they are prepared using the novel monomers I which contain specially selected molecular moieties B in a novel combination with selected molecular moieties C.

    摘要翻译: 可以重复地擦除并记录包含记录层(a)的新型激光 - 光学记录元件,其表现出对称性,铁电近晶液晶(Sc *)行为,使得它们可以在两个热力学稳定的光学可区分之间来回切换 通过施加外部电场,暴露于具有足够的发光功率的激光束的铁电近晶液晶SC *次序状态。 记录层(a)本身主要或全部由具有手性介晶侧基的新型聚合物P组成。 新型聚合物P使用通式I(I)的新型单体制备,其中R是氢,氯或甲基,A是柔性保持空间的长链分子部分,C是光学活性的手性 分子部分和B是由至少三个芳族核组成的介晶分子部分,其彼此线性或实质上线性地键合,或者它们使用含有特定选择的分子部分B的新型单体I与选择的分子 部分C.

    Purity of 1,6-hexanediol
    4.
    发明授权
    Purity of 1,6-hexanediol 失效
    1,6-己二醇的纯度

    公开(公告)号:US5767329A

    公开(公告)日:1998-06-16

    申请号:US860604

    申请日:1997-07-01

    CPC分类号: C07C29/88 C07C55/14 C07C59/01

    摘要: Impurities are separated from aqueous solutions of 1,6-hexanediol or 1,6-hexanediol precursors, such as adipic and 6-hydroxycaproic acid, by a process which comprises adding at least one carboxylic acid to a solution (a) of 1,6-hexanediol and subjecting this solution (a) or a solution (b) containing carboxylic acid(s) as precursor(s) of 1,6-hexanediol to a heat treatment at temperatures above room temperature in the absence of hydrogen.

    摘要翻译: PCT No.PCT / EP96 / 00023 Sec。 371日期1997年7月1日 102(e)1997年7月1日PCT 1996年1月4日PCT PCT。 WO96 / 20909 PCT出版物 日期1996年7月11日通过包括向溶液中加入至少一种羧酸的方法(1)将方法与1,6-己二醇或1,6-己二醇前体如己二酸和6-羟基己酸的水溶液分离, )的1,6-己二醇,并将该溶液(a)或含有羧酸的溶液(b)作为1,6-己二醇的前体进行热处理,在不高于室温的温度下进行热处理 氢。

    Monomers and their use for the production of a laser-optical recording
element which can be repeatedly erased and recorded on
    5.
    发明授权
    Monomers and their use for the production of a laser-optical recording element which can be repeatedly erased and recorded on 失效
    单体及其用于生产可以反复擦除并记录的激光光学记录元件

    公开(公告)号:US5212027A

    公开(公告)日:1993-05-18

    申请号:US814517

    申请日:1991-12-30

    摘要: Novel laser-optical recording elements which can be repeatedly erased and recorded on contain recording layers (a) which exhibit enantiotropic, ferroelectric smectic liquid crystalline (S.sub.c*) behavior, so that they can be switched back and forth between two thermodynamically stable, optically distinguishable ferroelectric smectic liquid crystalline S.sub.c* order states on exposure to a laser beam of sufficient luminous power, by applying an external electric field. The recording layers (a) themselves consist mainly or exclusively of novel polymers P having chiral mesogenic side groups. The novel polymers P are prepared using the novel monomers of the general formula I ##STR1## where R is hydrogen, chlorine or methyl, A is a flexible space-maintaining long-chain molecular moiety, and C is an optically active chiral molecular moiety and B is a mesogenic molecular moiety composed of at least three aromatic nuclei which are bonded linearly or virtually linearly to one another,or they are prepared using the novel monomers I which contain specially selected molecular moieties B in a novel combination with selected molecular moieties C.

    摘要翻译: 可以重复地擦除并记录包含记录层(a)的新型激光 - 光学记录元件,其表现出对称性,铁电近晶液晶(Sc *)行为,使得它们可以在两个热力学稳定的光学可区分之间来回切换 通过施加外部电场,暴露于具有足够发光功率的激光束的铁电近晶液晶Sc *阶数。 记录层(a)本身主要或全部由具有手性介晶侧基的新型聚合物P组成。 新型聚合物P使用通式I(I)的新型单体制备,其中R是氢,氯或甲基,A是柔性保持空间的长链分子部分,C是光学活性的手性 分子部分和B是由至少三个芳族核组成的介晶分子部分,其彼此线性或实质上线性地键合,或者它们使用含有特定选择的分子部分B的新型单体I与选择的分子 部分C.

    Preparation of 3-aminomethyl-3,5,5-trimethylcyclohexylamine
    10.
    发明授权
    Preparation of 3-aminomethyl-3,5,5-trimethylcyclohexylamine 失效
    3-氨基甲基-3,5,5-三甲基环己胺的制备

    公开(公告)号:US5756845A

    公开(公告)日:1998-05-26

    申请号:US608485

    申请日:1996-02-28

    CPC分类号: C07C209/48 C07C2101/14

    摘要: A process for the preparation of 3-aminomethyl-3,5,5-trimethylcyclohexylamine from 3-cyano-3,5,5-trimethylcyclohexanone which requires three spatially separated reaction spaces, in order to carry out the following three steps in sequence: a) reacting the 3-cyano-3,5,5-trimethylcyclohexanone with excess ammonia on acidic metal-oxide catalysts in a first reaction space at from 20.degree. to 150.degree. C. and from 50 to 300 bar, b) hydrogenating the resultant reaction products using hydrogen in a second reaction space in the presence of excess ammonia and preferably liquid ammonia on hydrogenation catalysts, optionally using basic components or on neutral or basic supports at from 50.degree. to 100.degree. C. and at from 50 to 300 bar, and c) hydrogenating the resultant reaction products in the presence of hydrogen and also ammonia in a third reaction space on hydrogenation catalysts, optionally using basic components or on neutral or basic supports at from 110.degree. to 160.degree. C. and at from 150 to 300 bar.These three steps in sequence provide a substantially complete reaction of the original 3-cyano-3,3,5-trimethylcyclohexanone reactant with a yield of 96% of the desired diamino product in which the cis-content of the diamine is 70%.

    摘要翻译: 从3-氰基-3,5,5-三甲基环己酮制备3-氨基甲基-3,5,5-三甲基环己胺的方法,其需要三个空间分离的反应空间,以便按顺序进行以下三个步骤:a )在20至150℃和50至300巴的第一反应空间中使3-氰基-3,5,5-三甲基环己酮与过量的氨在酸性金属氧化物催化剂上反应,b)将所得反应物氢化 在氢化催化剂存在下,在过量氨和优选液氨存在下在第二反应空间中使用氢的产物,任选使用碱性组分或在中性或碱性载体上在50至100℃和50至300巴条件下,以及 c)在氢化催化剂的第三反应空间中,在氢气和氨的存在下氢化所得反应产物,任选使用碱性组分或在中性或碱性载体上在110至160℃和150至300b ar。 这三个步骤依次提供原始3-氰基-3,3,5-三甲基环己酮反应物的基本上完全的反应物,其中二胺的顺式含量为70%的所需二氨基产物的产率为96%。