Process for preparing dinitrobenzophenones
    185.
    发明授权
    Process for preparing dinitrobenzophenones 失效
    二硝基二苯甲酮制备方法

    公开(公告)号:US4474989A

    公开(公告)日:1984-10-02

    申请号:US394261

    申请日:1982-07-01

    CPC classification number: C07C201/08 C07C2/68 C07C45/28 C07C2527/126

    Abstract: A process for preparing dinitrobenzophenones which comprises reacting benzene with ethylene in the presence of an alkylation catalyst to obtain an alkylation product containing unreacted benzene, ethylbenzene, polyethylbenzenes, 1,1-diphenylethane and heavier products, separating benzene, ethylbenzene and polyethylbenzenes from said alkylation product, recovering from the remainder of said alkylation product a fraction whose boiling points fall within the temperature range of about 260.degree. to about 290.degree. C., reacting said fraction with nitric acid at a temperature within the range of about 130.degree. to about 210.degree. C., wherein the molar ratio of nitric acid to said fraction is in the range of about 3:1 to about 8:1, and thereafter reacting the total resulting reaction product with nitric acid in oleum to obtain a nitration product predominating in dinitrobenzophenones.

    Abstract translation: 一种制备二硝基二苯甲酮的方法,其包括在烷基化催化剂存在下使苯与乙烯反应,得到含有未反应苯,乙苯,聚乙苯,1,1-二苯基乙烷和较重产物的烷基化产物,从所述烷基化产物中分离苯,乙苯和聚乙基苯 从所述烷基化产物的剩余部分中回收沸点落在约260℃至约290℃的温度范围内的馏分,使所述馏分与硝酸在约130至约210℃的温度范围内反应。 其中硝酸与所述馏分的摩尔比在约3:1至约8:1的范围内,然后使总产生的反应产物与硝酸在发烟硫酸中反应,得到主要在二硝基二苯甲酮中的硝化产物。

    Process for producing o-nitrobenzaldehyde
    186.
    发明授权
    Process for producing o-nitrobenzaldehyde 失效
    邻硝基苯甲醛生产方法

    公开(公告)号:US4463195A

    公开(公告)日:1984-07-31

    申请号:US484842

    申请日:1983-04-14

    CPC classification number: C07C201/12

    Abstract: Ortho-nitrobenzaldehyde, a well known compound suitable as an indicator and as an intermediate for many organic syntheses including production of pharmaceuticals, is obtained by contacting a C.sub.1 -C.sub.4 lower alkyl ester of o-nitrophenyl pyruvic acid in the form of its enolate, i.e. the enol salt or enol ester, with hydrogen peroxide; the enol salt can be the enolate of an alkali metal, an alkaline earth metal or of aluminum, and the enol ester can be the ester formed by the enolic hydroxyl and formic, acetic, propionic or butyric acid.

    Abstract translation: 通过使其以烯醇化合物形式的邻硝基苯基丙酮酸的C 1 -C 4低级烷基酯接触,即作为指示剂的公知化合物和作为包括药物生产在内的许多有机合成的中间体的正 - 硝基苯甲醛,即 烯醇盐或烯醇酯,与过氧化氢; 烯醇盐可以是碱金属,碱土金属或铝的烯醇化物,烯醇酯可以是由烯醇羟基和甲酸,乙酸,丙酸或丁酸形成的酯。

    Process for preparation of di- or trifluoromethoxyphenyl ketones or di-
or trifluoromethylthiophenyl ketones
    189.
    发明授权
    Process for preparation of di- or trifluoromethoxyphenyl ketones or di- or trifluoromethylthiophenyl ketones 失效
    制备二 - 或三氟甲氧基苯基酮或二 - 或三氟甲硫基苯基酮的方法

    公开(公告)号:US4438043A

    公开(公告)日:1984-03-20

    申请号:US392886

    申请日:1982-06-28

    Applicant: Michel Desbois

    Inventor: Michel Desbois

    CPC classification number: C07C45/008 C07C323/00 C07C45/43

    Abstract: A process for the preparation of di- or trifluoromethoxyphenyl ketones or di- or trifluoromethylthiophenyl ketones, characterized in that, in a first stage, a di- or trihalomethoxybenzene or a di- or trihalomethylthiobenzene is reacted with a trihalomethylated aromatic or aliphatic compound in the presence of boron trifluoride in an amount such that the absolute pressure of boron trifluoride within the reaction vessel exceeds 1 bar, and in the presence of hydrofluoric acid as a solvent and in that, in a second stage, the product of the first stage is hydrolyzed. The resultant products are useful as intermediates in the synthesis of compounds having a pharmaceutical or phytosanitary (e.g., herbicidal) activity.

    Abstract translation: 一种制备二 - 或三氟甲氧基苯基酮或二 - 或三氟甲硫基苯基酮的方法,其特征在于,在第一阶段中,二 - 或三卤甲氧基苯或二 - 或三卤代甲硫基苯与三卤甲基化芳族或脂族化合物在存在下反应 的三氟化硼的量使得反应容器内的三氟化硼的绝对压力超过1巴,在作为溶剂的氢氟酸的存在下,在第二阶段中,第一阶段的产物被水解。 所得产物可用作合成具有药物或植物检疫(例如除草)活性的化合物的中间体。

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