Process for preparing N-alkylcarbazoles
    2.
    发明授权
    Process for preparing N-alkylcarbazoles 失效
    制备N-烷基咔唑的方法

    公开(公告)号:US5902884A

    公开(公告)日:1999-05-11

    申请号:US21981

    申请日:1998-02-11

    CPC分类号: C07D209/88 C07D209/86

    摘要: Process for preparing N-alkylcarbazolesThe present invention relates to a process for preparing N-alkylcarbazoles of the formula I ##STR1## where R.sup.1 is (C.sub.1 -C.sub.6)-alkyl andY is hydrogen, (C.sub.1 -C.sub.6)-alkyl, (C.sub.1 -C.sub.6)-alkoxy, nitro or halogen, by reacting a carbazole of the formula II ##STR2## with an alkyl halide of the formula IIIR.sup.1 -X IIIwhere X is a halogen atom,in an inert solvent in the presence of an inorganic base and a catalyst of the formula IVR.sup.2 R.sup.3 N-(CH.sub.2).sub.n -NR.sup.4 R.sup.5 IVwheren is an integer from 2 to 8,R.sup.2, R.sup.3 and R.sup.4 are, independently of one another, hydrogen or (C.sub.1 -C.sub.4)-alkyl andR.sup.5 is hydrogen, (C.sub.1 -C.sub.4)-alkyl, amino-(C.sub.1 -C.sub.4)-alkyl or N,N-di(C.sub.1 -C.sub.4)-alkylamino-(C.sub.1 -C.sub.4)-alkyl.

    摘要翻译: 制备N-烷基咔唑的方法本发明涉及制备式I的N-烷基咔唑的方法,其中R 1为(C 1 -C 6) - 烷基且Y为氢,(C 1 -C 6) - 烷基,(C 1 -C 6) - 烷氧基,硝基或卤素,在惰性溶剂中,在惰性溶剂中,在无机碱和式IVR2R3N-的催化剂的存在下,使式II的咔唑与式IIIR1-XIII的烷基卤反应,其中X是卤素原子, (CH2)n-NR4R5IV其中n为2至8的整数,R2,R3和R4彼此独立地为氢或(C1-C4) - 烷基,R5为氢,(C1-C4) - 烷基, 氨基 - (C 1 -C 4) - 烷基或N,N-二(C 1 -C 4) - 烷基氨基 - (C 1 -C 4) - 烷基。

    Separation of m- and p-dichlorobenzene
    4.
    发明授权
    Separation of m- and p-dichlorobenzene 失效
    对 - 二苯并苯的分离

    公开(公告)号:US5152875A

    公开(公告)日:1992-10-06

    申请号:US681891

    申请日:1991-04-08

    CPC分类号: C07C17/386

    摘要: A process for separating m- and p-dichlorobenzene by extractive rectification with an extractant and removal of this extractant. Using as extractant an alkylene carbonate of the formula ##STR1## where R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are identical to or different from one another and each is hydrogen, methyl or ethyl, with the proviso that together the radicals R.sup.1 to R.sup.4 do not contain more than 6 carbon atoms.The process of the invention makes it possible to separate off the m-isomer in high purity.

    摘要翻译: 通过萃取剂萃取精馏分离间二氯和对二氯苯并除去该萃取剂的方法。 使用作为萃取剂的式(I)的碳酸亚烷酯,其中R 1,R 2,R 3和R 4彼此相同或不同,并且各自为氢,甲基或乙基,条件是基团R 1至R 4 不含6个以上碳原子。 本发明的方法使得可以以高纯度分离出m-异构体。

    Preparation of trans-thiazineindigo pigments
    7.
    发明授权
    Preparation of trans-thiazineindigo pigments 失效
    反噻嗪染料的制备

    公开(公告)号:US06649758B2

    公开(公告)日:2003-11-18

    申请号:US09886569

    申请日:2001-06-21

    IPC分类号: C07D27916

    CPC分类号: C09B7/00

    摘要: A process for preparing symmetrical or asymmetrical trans-thiazineindigo pigments of the formula (1) which comprises a) condensing, in an aqueous medium, a compound of the formula (2) with a compound of the formula (3a) or (3b) or a compound of the formula (4) with a compound of the formula (3a) and/or (3b)  by maintaining the reaction mixture at a temperature between 30 and 65° C. for at least 1 hour and then b) maintaining the reaction mixture at a temperature between 100 and 180° C. and a pressure between 2 and 50 bar for at least 1 hour in the presence of an amide.

    摘要翻译: 制备式(1)的对称或不对称的反噻嗪靛色素的方法,其包括:a)在水性介质中将式(2)的化合物与式(3a)或(3b)的化合物或 将式(4)的化合物与式(3a)和/或(3b)的化合物通过将反应混合物保持在30至65℃的温度至少1小时,然后b)将反应混合物保持在 温度为100至180℃,压力为2至50巴,在酰胺存在下至少1小时。