CONTINUOUS PROCESS OF PREPARING BROMOPICRIN
    71.
    发明申请
    CONTINUOUS PROCESS OF PREPARING BROMOPICRIN 有权
    连续制备BROMOPICRIN的方法

    公开(公告)号:US20100204528A1

    公开(公告)日:2010-08-12

    申请号:US12601547

    申请日:2008-05-26

    CPC classification number: C07C201/12 C07C205/08

    Abstract: A continuous process of preparing bromopicrin is disclosed. The process is effected by transferring a continuous flow of a first mixture and a continuous flow of a second mixture into a first reactor, the first mixture containing nitromethane and bromine and the second mixture containing an aqueous solution of an alkaline substance, to thereby obtain a reaction mixture which comprises bromopicrin in said first reactor; and collecting the bromopicrin from the reaction mixture. Highly pure bromopicrin obtained by this process is also disclosed.

    Abstract translation: 公开了制备溴氰菊酯的连续方法。 该方法通过将第一混合物的连续流和第二混合物的连续流转移到第一反应器中,第一混合物含有硝基甲烷和溴,第二混合物含有碱性物质的水溶液,从而获得 在所述第一反应器中包含溴化苦素的反应混合物; 并从反应混合物中收集溴氰菊酯。 还公开了通过该方法获得的高纯度溴氰菊酯。

    Process for Preparing Substituted Biphenyls
    73.
    发明申请
    Process for Preparing Substituted Biphenyls 失效
    制备取代联苯的方法

    公开(公告)号:US20090005597A1

    公开(公告)日:2009-01-01

    申请号:US12087345

    申请日:2007-05-31

    CPC classification number: C07C201/12 C07C209/68 C07C211/52 C07C205/12

    Abstract: A process for preparing substituted biphenyls of the formula I in which the substituents are defined as follows: X is fluorine or chlorine; R1 is nitro, amino or NHR3; R2 is cyano, nitro, halogen, C1-C6-alkyl, C1-C6-alkenyl, C1-C6-alkynyl, C1-C6-alkoxy, C1-C6-haloalkyl, C1-C6-alkylcarbonyl or phenyl; R3 is C1-C4-alkyl, C1-C4-alkenyl or C1-C4-alkynyl; n is 1, 2 or 3, where in case that n is 2 or 3, the R2 radicals may also be different, which comprises reacting the compound of the formula II in which Hal is halogen and X and R1 are as defined above, in the presence of a base and of a palladium catalyst selected from the group of: a) palladium-triarylphosphine or -trialkylphosphine complex with palladium in the zero oxidation state, b) salt of palladium in the presence of triarylphospine or trialkylphosphine as a complex ligand or c) metallic palladium, optionally applied to support, in the presence of triarylphosphine or trialkylphosphine, in a solvent, with a diphenylborinic acid (III) in which R2 and n are as defined above, where the triarylphosphines or trialkylphosphines used may be substituted.

    Abstract translation: 制备式I取代的联苯的方法,其中取代基定义如下:X是氟或氯; R1是硝基,氨基或NHR3; R2是氰基,硝基,卤素,C1-C6-烷基,C1-C6-烯基,C1-C6-炔基,C1-C6-烷氧基,C1-C6-卤代烷基,C1-C6-烷基羰基或苯基; R3是C1-C4-烷基,C1-C4-烯基或C1-C4-炔基; n为1,2或3,其中在n为2或3的情况下,R2基团也可以不同,其包括使Hal为卤素的化合物与X和R 1如上所定义的化合物反应在 存在碱和钯催化剂,其选自:a)钯 - 三芳基膦或三烷基膦配合物与钯在零氧化状态,b)钯在三芳基膦或三烷基膦作为络合配体的存在下的盐,或 c)金属钯,任选地在三芳基膦或三烷基膦存在下,在溶剂中与其中R 2和n如上定义的二苯基硼酸(III)反应,其中所用的三芳基膦或三烷基膦可以被取代。

    Process for the preparation of fluorinated aromatic compounds
    78.
    发明授权
    Process for the preparation of fluorinated aromatic compounds 失效
    氟化芳族化合物的制备方法

    公开(公告)号:US6114589A

    公开(公告)日:2000-09-05

    申请号:US170381

    申请日:1998-10-13

    CPC classification number: C07C253/30 C07B39/00 C07C201/12 C07C45/63

    Abstract: The invention relates to a process for the preparation of fluorinated compoundsAz.sub.x ArF.sub.w Cl.sub.(y-w) R.sub.z (1)in which Az is a radical --F, --Cl, --Br, --NO.sub.2, --CN, --CF.sub.3, --CCl.sub.3, --CHO, --CO(C.sub.n H.sub.2n+1), --COX or --SO.sub.2 X, where X is F, Cl or Br, x is an integer from 1 to 3, Ar is a phenyl radical, pyridyl radical or naphthyl, w is an integer from 1 to y, y is an integer from 1 to 5, R is H, an alkyl radical or an alkoxy radical having from 1 to 10 carbon atoms, z is an integer from 1 to 5, (x+y+z) is the number of all substitutable valences on the radical Ar, which comprises reacting a compoundAz.sub.x ArCl.sub.y R.sub.z (2),with an alkali metal fluoride in the presence of a component a) or a mixture of component a) and at least one of components b), c), d) and/or e), component a) being one or more quaternary ammonium compounds which contain one or more radicals --(C.sub.m H.sub.2m O)R.sup.5, component b) being an amidophosphonium salt, component c) being a quaternary ammonium salt, component d) being a quaternary phosphonium salt, component e) being a polyether, and carrying out the reaction at from 50 to 250.degree. C., removing the compound of the formula (1) formed during the reaction by distillation, and the compound of the formula (2) is fed to the reaction mixture at a rate corresponding to the rate at which the compound of the formula (1) is removed.

    Abstract translation: 本发明涉及一种制备氟化化合物的方法,其中Z 1为基团-F,-Cl,-Br,-NO 2,-CN,-CF 3,-CCl 3,-CHO - , - CO(CnH2n + 1),-COX或-SO2X,其中X为F,Cl或Br,x为1至3的整数,Ar为苯基,吡啶基或萘基,w为1至y的整数 y为1〜5的整数,R为H,烷基或碳原子数为1〜10的烷氧基,z为1〜5的整数,(x + y + z)为全部数 在基团Ar上具有可取代价,其包括使化合物AZxArClyRz(2)与碱金属氟化物在组分a)或组分a)和组分b),c),d)中的至少一种的存在下反应, 和/或e)组分a)是一种或多种含有一个或多个基团的季铵化合物 - (CmH2mO)R5,组分b)是酰胺鏻盐,组分c)是季铵盐,组分d)是 季鏻盐,组分e)b 取代聚醚,并在50-250℃下进行反应,通过蒸馏除去反应期间形成的式(1)化合物,将式(2)化合物加入到反应混合物中 对应于除去式(1)的化合物的速率的速率。

    Removal of dinitrotoluene from process water
    80.
    发明授权
    Removal of dinitrotoluene from process water 失效
    从工艺用水中除去二硝基甲苯

    公开(公告)号:US5763696A

    公开(公告)日:1998-06-09

    申请号:US827326

    申请日:1997-03-26

    CPC classification number: B01D3/34

    Abstract: Reduction of dinitrotoluene impurity in water is achieved by distillation in the presence of nitric acid. A suitable process for such reduction comprises (a) contacting said composition with nitric acid to provide a nitric acid-containing composition, (b) distilling at least a portion of said water in said nitric acid-containing composition to provide vaporized water containing a reduced concentration of said dinitrotoluene, and (c) separating said vaporized water from said nitric acid-containing composition.

    Abstract translation: 在硝酸存在下通过蒸馏来还原二硝基甲苯杂质。 用于这种还原的合适方法包括(a)使所述组合物与硝酸接触以提供含硝酸的组合物,(b)在所述含硝酸的组合物中蒸馏至少一部分所述水以提供含有还原剂的蒸发水 所述二硝基甲苯的浓度,和(c)从所述含硝酸的组合物中分离所述蒸发的水。

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