Fractionation of c12 bicycle aromatic hydrocarbons by 2-chloro,4-nitrobenzoic acid complex formation
    1.
    发明授权
    Fractionation of c12 bicycle aromatic hydrocarbons by 2-chloro,4-nitrobenzoic acid complex formation 失效
    通过2-氯代,4-硝基苯甲酸复合物形成C12BICYCLE芳香烃的分离

    公开(公告)号:US3665044A

    公开(公告)日:1972-05-23

    申请号:US3665044D

    申请日:1970-05-01

    Applicant: SUN OIL CO

    Inventor: SCOTT KENNETH A

    CPC classification number: C07C7/152 C07C15/24

    Abstract: Mixtures of C12 bicyclic aromatic hydrocarbons containing dimethylnaphthalenes are difficult to fractionate by conventional techniques such as distillation or crystallization. However, by dissolving 2-chloro, 4-nitrobenzoic acid in such a mixture at an elevated temperature, followed by subsequent cooling, a solid complex of said acid and certain hydrocarbons is formed. Separation of the solid complex from the cooled mixture and its subsequent decomposition results in a product that is substantially richer in those dimethylnaphthalenes which have greater tendency to form such complexes. Upon further processing, these dimethylnaphthalenes have utility in the production of dyes.

    Separation of 2,6-and 2,7-dmn eutectic via 2,6-dimethyltetrahydronaphthalene crystallization
    3.
    发明授权
    Separation of 2,6-and 2,7-dmn eutectic via 2,6-dimethyltetrahydronaphthalene crystallization 失效
    通过2,6-二甲基四氢呋喃晶体结晶分离2,6和2,7- DMN保护

    公开(公告)号:US3594436A

    公开(公告)日:1971-07-20

    申请号:US3594436D

    申请日:1969-02-03

    Applicant: SUN OIL CO

    Abstract: ESSENTIALLY ALL OF THE 2,6-DIMETHYLNAPHTHALENE (DMN) CONTAINED IN THE 2,6-/2,7-DIMETHYLNAPHTHALENE EUTECTIC MIXTURE CAN BE RECOVERED BY HYDROGENATING THE EUTECTIC MIXTURE TO PRODUCE A MIXTURE OF 2,6- AND 2,7-DIMETHYLTETRALIN (DMT). THE 2,6/2,7-DMT ALSO FORMS A EUTECTIC, HOWEVER, IT IS AT A DIFFERENT RATIO THAN THE 2,6/2,7-DMN. THE SHIFT IS IN FAVOR OF GREATER 2,7-DMT IN THE EUTECTIC THUS THERE IS FREE 2,6-DMT THAT CAN BE RECOVERED FROM THIS MIXTURE. 2,6-DMT CAN BE RECOVERED IN HIGH YIELDS AND HIGH PURITY BY CAREFULLY CONTROLLING THE TEMPERATURE OF CRYSTALLIZATION AT THE LOWEST TEMPERATURE DETERMINED FROM FIG. 3 AT WHICH ALL OF THE 2,6-/2,7-DMT EUTECTIC IS SOLUBLE IN THE LIQUIDS PRESENT. FOR EXAMPLE, A HYDROGENATED 2,6-/2,7-DMN EUTECTIC FEED CONTAINING

    WT. PERCENT 2,6-DMT 30 2,7-DMT 30 OTHER LIQUID AROMATICS 40

    WILL HAVE A EUTECTIC OF 2,6-/2,7-DMT IN THE WEIGHT RATIO OF .538. THUS, THE EUTECTIC REPRESENTS 46.2% OF THE INCOMING FEED. TO USE FIG. 3, THE WEIGHT PERCENT OF EUTECTIC IS CALCULATED ON TOTAL FEED EXCLUDING THE FREE 2,6-DMT IN THIS CASE THE WEIGHT PERCENT OF EUTECTIC TO BE DISSOLVED IS CALCULATED TO BE 53.6 WT. PERCENT. FROM FIG .3, 53.66 WT. PERCENT EUTECTIC IS SOLUBLE AT -51*C. THE TEMPERATURE OF CRYSTALLIZATION SHOULD BE NO LESS THAN -51*C. ($2*C.) TO AVOID CRYSTALLIZATION OF THE 2,6-/2,7-DMT EUTECTIC AND NO MORE THAN -51*C. ($2*C.) TO AVOID DISSOLVING FREE 2,6-DMT.

    Preparation of 2-pyrrolidinone
    5.
    发明授权
    Preparation of 2-pyrrolidinone 失效
    2-吡咯烷酮的制备

    公开(公告)号:US3681387A

    公开(公告)日:1972-08-01

    申请号:US3681387D

    申请日:1970-10-16

    Applicant: SUN OIL CO

    CPC classification number: C07D201/02 C07D201/08

    Abstract: An improved process for preparing 2-pyrrolidinone at relatively low pressures which comprises reduction of succinimide in an aqueous system at temperatures of about 225* to 275* C., at a pressure in the range of about 1,200 to 1,500 p.s.i.g. and in the presence of a supported palladium catalyst.

    Abstract translation: 一种用于在相对低的压力下制备2-吡咯烷酮的改进方法,其包括在约225-275℃的温度下在水性体系中还原琥珀酰亚胺,压力范围为约1,200至1,500p.s.i。 并在负载型钯催化剂存在下进行。

    Fractionation of eutectic mixtures of dimethylnapthalenes by dianhydride complexation
    6.
    发明授权
    Fractionation of eutectic mixtures of dimethylnapthalenes by dianhydride complexation 失效
    通过二氢吡喃复合物分离二甲基联苯的保护性混合物

    公开(公告)号:US3665045A

    公开(公告)日:1972-05-23

    申请号:US3665045D

    申请日:1970-05-01

    Applicant: SUN OIL CO

    CPC classification number: C07C7/152 C07C15/24

    Abstract: Binary eutectics of dimethylnapthalenes having each methyl group at a Beta position cannot be fractionated by crystallization and are difficult to fractionate by distillation. However, by dissolving the normally solid eutectic in an inert solvent and contacting the resulting solution with a dianhydride of 1,2,4,5,benzenetetracarboxylic acid or a dianhydride of 1,2,3,4benzenetetracarboxylic acid, a solid complex is formed. Separation of the solid complex and its subsequent decomposition results in a complexate that is substantially richer in a dimethylnapthalene which is preferentially complexed. Dimethylnaphthalenes are oxidized to naphthalenecarboxylic acids which are used in the production of dyes and pigments.

    Fractionation of c12 bicyclic aromatic hydrocarbons by di or trianhydride complex formation
    7.
    发明授权
    Fractionation of c12 bicyclic aromatic hydrocarbons by di or trianhydride complex formation 失效
    通过DI或三乙酸复合物形成C12双环芳香烃的分离

    公开(公告)号:US3665043A

    公开(公告)日:1972-05-23

    申请号:US3665043D

    申请日:1970-05-01

    Applicant: SUN OIL CO

    CPC classification number: C07C7/152 C07C15/24

    Abstract: Mixtures of C12 bicyclic aromatic hydrocarbons containing dimethylnaphthalenes are difficult to fractionate by conventional techniques such as distillation or crystallization. However, by contacting such mixtures with the dianhydride of 1,2,4,5benzenetetracarboxylic acid, the dianhydride of 1,2,3,4benzenetetracarboxylic acid or the trianhydride of 1,2,3,4,5,6,benzenehexacarboxylic acid, a solid complex of certain hydrocarbons and the polyanhydride is formed. Separation of the solid complex and its subsequent decomposition results in a complexate that is substantially richer in those dimethylnaphthalenes which are preferentially complexed. Upon further processing these dimethylnaphthalenes have utility in the production of dyes.

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