Isolation of dinitroanthraquinone having a high content of .alpha.,.alpha.-
d
    244.
    发明授权
    Isolation of dinitroanthraquinone having a high content of .alpha.,.alpha.- d 失效
    具有高含量{60,{60-二硝基化合物的二硝基蒽醌的分离

    公开(公告)号:US4042604A

    公开(公告)日:1977-08-16

    申请号:US686365

    申请日:1976-05-14

    CPC classification number: C07C225/34

    Abstract: A process for the isolation of mixtures of 1,5-dinitroanthraquinone and 1,8-dinitroanthraquinone which have a high content of .alpha.,.alpha.'-dinitroanthraquinones by heating a suspension of the crude dinitroanthraquinone mixture in certain organic liquids at from 60.degree. to 200.degree. C until solution equilibrium has been set up, and separating the undissolved material from the solution. The undissolved material contains more than 90% and as a rule more than 95% by weight of 1,5-dinitroanthraquinone and 1,8-dinitroanthraquinone. The pure mixture of 1,5-dinitroanthraquinone and 1,8-dinitroanthraquinone may be used for the manufacture of dyes.

    Abstract translation: 通过在60°至200°的某些有机液体中加热粗二硝基蒽醌混合物的悬浮液,分离具有高α,α'-二硝基蒽醌含量的1,5-二硝基蒽醌和1,8-二硝基蒽醌的混合物的方法 直到溶液平衡已经建立,并将未溶解的材料与溶液分离。 未溶解的材料含有超过90%且通常超过95重量%的1,5-二硝基蒽醌和1,8-二硝基蒽醌。 1,5-二硝基蒽醌和1,8-二硝基蒽醌的纯混合物可用于制备染料。

    Process for the preparation of 2-nitrobenzaldehyde
    248.
    发明授权
    Process for the preparation of 2-nitrobenzaldehyde 失效
    制备2-硝基苯甲醛的方法

    公开(公告)号:US3996289A

    公开(公告)日:1976-12-07

    申请号:US557297

    申请日:1975-03-11

    Applicant: Horst Meyer

    Inventor: Horst Meyer

    CPC classification number: C07C205/44 C07C201/12

    Abstract: 2-NITROBENZALDEHYDE, A VALUABLE CHEMICAL INTERMEDIATE, IS PREPARED THROUGH THE OXIDATION OF AN ALKALI METAL SALT OF 2-NITROPHENYLPYRUVIC ACID WITH POTASSIUM PERMANGANATE IN AN ALKALINE MEDIUM. Advantageously the requisite starting material is prepared directly by the reaction of 2-nitrotoluene and a diester of oxalic acid in the presence of an alcoholate and is then subjected to the oxidation without isolation. In a preferred embodiment the oxidation reaction mixture is acidified to convert the manganese-(IV) oxide to soluble maganese-(II) salts with concurrent conversion of oxalic acid to carbon dioxide. The process is industrially attractive in terms of the high yield, the availability of starting material and the ease of the manipulative steps involved.

    Abstract translation: 2-NITROBENZALDEHYDE,一种有价值的化学中间体,是通过在碱性介质中用硫酸钾处理2-硝基戊酸的碱金属盐来制备的。 有利的是,必需的原料直接通过在醇化物存在下由2-硝基甲苯与草酸二酯的反应制备,然后在不分离的条件下进行氧化。 在优选的实施方案中,将氧化反应混合物酸化以将锰(IV)氧化物转化为可溶性的锰 - (II)盐,同时将草酸转化为二氧化碳。 该方法在高产率,起始材料的可用性和所涉及的操纵步骤的容易性方面在工业上具有吸引力。

    Dinitration of nitrobenzotrifluoride
    250.
    发明授权
    Dinitration of nitrobenzotrifluoride 失效
    二硝基三氟甲苯的硝化

    公开(公告)号:US3984488A

    公开(公告)日:1976-10-05

    申请号:US580505

    申请日:1975-05-23

    Inventor: Barton Milligan

    CPC classification number: C07C201/12

    Abstract: This invention relates to an improvement in an process for dinitrating 3-nitrobenzotrifluoride and 4-hal0-3-nitrobenzotrifluoride compounds wherein the mononitrobenzotrifluoride composition is contacted with a mixture comprising sulfuric and nitric acid. The improvement constituting the basis of this invention comprises carrying out the dinitration with the sulfuric acid being present in at least a catalytic proportion but not exceeding about 65 mole percent in said mixture.

    Abstract translation: 本发明涉及三硝基三氟甲苯和4-卤代-3-硝基三氟甲苯化合物的二硝化方法的改进,其中一硝基三氟甲苯组合物与包含硫酸和硝酸的混合物接触。 构成本发明基础的改进包括以所述混合物中至少催化比例但不超过约65摩尔%的硫酸进行二硝化。

Patent Agency Ranking