Separation of 3,3-dimethylacrolein and -methyl-3-buten-1-ol by azeotropic distillation with water and glycerol
    22.
    发明授权
    Separation of 3,3-dimethylacrolein and -methyl-3-buten-1-ol by azeotropic distillation with water and glycerol 失效
    通过与水和甘油共沸蒸馏分离3,3-二甲基丙烯醛和 - 甲基-3-丁烯-1-醇

    公开(公告)号:US3894916A

    公开(公告)日:1975-07-15

    申请号:US39282173

    申请日:1973-08-29

    Applicant: BASF AG

    CPC classification number: C07C45/84 C07C47/21

    Abstract: A process for separating, by distillation, a mixture consisting essentially of 3,3-dimethylacrolein and 3-methyl-3-buten-1-ol, wherein the mixture to be separated is distilled in the presence of water and glycerol, the 3,3-dimethyl-acrolein first being distilled off azeotropically with water and the 3-methyl-3-buten1-ol then being separated, as an azeotropic mixture with water, from the higher-boiling glycerol. It is also possible to isolate the 3,3-dimethylacrolein by distillation if the 3-methyl-3-buten1-ol is partially replaced by 3-methyl-2-buten-1-ol. The 3,3dimethylacrolein, which can be isolated in pure form by the process of the invention, is a valuable intermediate for the synthesis of natural substances such as citral, vitamin A and chrysanthemic acid.

    Abstract translation: 通过蒸馏分离基本上由3,3-二甲基丙烯醛和3-甲基-3-丁烯-1-醇组成的混合物的方法,其中待分离的混合物在水和甘油的存在下蒸馏, 首先与水共沸蒸馏出3-三甲基 - 丙烯醛,然后将3-甲基-3-丁烯-1-醇与较高沸点甘油作为与水的共沸混合物分离。 如果3-甲基-3-丁烯-1-醇部分被3-甲基-2-丁烯-1-醇代替,也可以通过蒸馏分离3,3-二甲基丙烯醛。 可以通过本发明的方法以纯形式分离的3,3-二甲基丙烯醛是合成天然物质如柠檬醛,维生素A和菊酸的有价值的中间体。

    Production of 2-phenyl-3-nitrobutyric acid compounds
    26.
    发明授权
    Production of 2-phenyl-3-nitrobutyric acid compounds 失效
    2-苯基-3-硝基丁酸化合物的制备

    公开(公告)号:US3887617A

    公开(公告)日:1975-06-03

    申请号:US26643272

    申请日:1972-06-26

    Applicant: BASF AG

    CPC classification number: C07C201/12 C07C231/12 C07C205/53 C07C233/11

    Abstract: The production of compounds of 2-phenyl-3-nitrobutyric acid by reaction of 1-phenyl-2-nitroethenes with lithium carboxamides. The compounds which can be prepared according to the process of the invention are valuable starting materials for the production of dyes and pharmaceuticals.

    Abstract translation: 2-苯基-3-硝基丁酸的化合物通过1-苯基-2-硝基乙烯与氨基甲酰胺的反应生成。 可根据本发明方法制备的化合物是用于生产染料和药物的有价值的原料。

    Process for the production of 1-amino-4-nitroanthraquinone-2-carboxylic esters
    27.
    发明授权
    Process for the production of 1-amino-4-nitroanthraquinone-2-carboxylic esters 失效
    1-氨基-4-硝基蒽醌-2-羧酸酯的制备方法

    公开(公告)号:US3887591A

    公开(公告)日:1975-06-03

    申请号:US41242173

    申请日:1973-11-02

    Applicant: BASF AG

    CPC classification number: C09B1/22 C07D265/12

    Abstract: The production of 1-amino-4-nitroanthraquinone-2-carboxylic esters by reaction of 1,2-dihydro-6-nitro-7,8-diphthaloyl-3,1,4Hbenzoxazone-4 with an alcohol in the presence of an acid catalyst. Pure carboxylic esters are immediately obtained in a high yield previous isolation of the carboxylic acid.

    Abstract translation: 通过1,2-二氢-6-硝基-7,8-二邻苯二甲酰基-3,1,4H-苯并恶嗪-4与醇在存在下反应生产1-氨基-4-硝基蒽醌-2-羧酸酯 酸催化剂。 立即以高产率先前分离羧酸得到纯羧酸酯。

    Production of pure 1-amino-4-nitroanthraquinone-2-carboxylic acid
    29.
    发明授权
    Production of pure 1-amino-4-nitroanthraquinone-2-carboxylic acid 失效
    纯1-氨基-4-硝基蒽醌-2-羧酸的制备

    公开(公告)号:US3886188A

    公开(公告)日:1975-05-27

    申请号:US39917473

    申请日:1973-09-20

    Applicant: BASF AG

    CPC classification number: C09B1/22

    Abstract: An improvement in the process for the production of 1-amino-4nitroanthraquinone-2-carboxylic acid from 1-aminoanthraquinone-2carboxylic acid by reaction with formaldehyde in concentrated sulfuric acid and nitration of the reaction product into 1,2dihydro-6-nitro-7,8-diphthaloyl-3,1,4H-benzoxazone-4 followed by hydrolysis of the same. The improvement consists in precipitating the benzoxazone derivative by adding a precipitant, hydrolyzing the isolated benzoxazone derivative in aqueous solution and precipitating the 1-amino-4-nitro-anthraquinone-2-carboxylic acid from the alkaline solution by acidification. 1-amino-4nitroanthraquinone-2-carboxylic acid is obtained in a purity of 95 percent by weight or more.

    Abstract translation: 通过在浓硫酸中与甲醛反应,由1-氨基蒽醌-2-羧酸生产1-氨基-4-硝基蒽醌-2-羧酸的方法的改进,并将反应产物硝化成1,2-二氢 -6-硝基-7,8-二邻苯二甲酰基-3,1,4H-苯并恶嗪-4,然后水解。 改进在于通过添加沉淀剂沉淀苯并恶嗪衍生物,水解分离的苯并恶嗪衍生物并通过酸化从碱性溶液中沉淀出1-氨基-4-硝基 - 蒽醌-2-羧酸。 得到纯度为95重量%以上的1-氨基-4-硝基蒽醌-2-羧酸。

    Manufacture of aliphatic alcohols
    30.
    发明授权
    Manufacture of aliphatic alcohols 失效
    脂肪醇的制造

    公开(公告)号:US3880940A

    公开(公告)日:1975-04-29

    申请号:US41807073

    申请日:1973-11-21

    Applicant: BASF AG

    CPC classification number: B01J23/883 C07C29/141 C07C31/12

    Abstract: Manufacture of saturated aliphatic alcohols by hydrogenation of saturated aliphatic aldehydes at temperatures of from 140* to 230*C at pressures of from 50 to 350 atmospheres in the presence of catalysts containing from 5 to 15% by weight nickel and 5 to 20% by weight molybdenum supported on silicic acid, in which process catalysts are used which have been obtained by heating silicic acid carrier materials to temperatures of from 700* to 1200*C, impregnating the resulting silicic acid carrier materials with nickel and molybdenum salts, drying the resulting material with or without further heating to temperatures of from 200* to 500*C and subsequently treating the product with hydrogen at elevated temperature in conventional manner. The alcohols obtained are used as solvents or for the manufacture of plasticizers for polyvinyl chloride.

    Abstract translation: 在含有5至15重量%镍和5至20重量%催化剂的催化剂存在下,通过在140至230℃的温度下,在50至350大气压的压力下,饱和脂族醛的氢化制备饱和脂族醇 负载在硅酸上的钼,其中使用通过将硅酸载体材料加热至700℃至1200℃的温度而获得的工艺催化剂,用镍和钼盐浸渍所得硅酸载体材料,干燥所得材料 有或没有进一步加热至200℃至500℃的温度,随后以常规方式在升高的温度下用氢处理产物。 所得的醇用作溶剂或制造聚氯乙烯的增塑剂。

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