Catalyzed oxime conversions
    172.
    发明授权
    Catalyzed oxime conversions 失效
    催化肟转化

    公开(公告)号:US4883915A

    公开(公告)日:1989-11-28

    申请号:US35868

    申请日:1987-04-08

    CPC classification number: C07D201/04

    Abstract: A process for the catalyzed conversion fo oximes such as cyclohexanone oxime to amides such as caprolactam via a high conversion, high selectivity, long catalyst lifetime reaction over a HAMS-1B crystalline borosilicate-based catalyst composition.

    Abstract translation: 通过HAMS-1B结晶硼硅酸盐基催化剂组合物的高转化率,高选择性,长的催化剂寿命反应,催化转化如环己酮肟向酰胺如己内酰胺转化的方法。

    Reaction of ketoximes with carboxylic acid amide-sulfur trioxide complexes
    175.
    发明授权
    Reaction of ketoximes with carboxylic acid amide-sulfur trioxide complexes 失效
    羧酸与三羧酸酰硫化物复合物的反应

    公开(公告)号:US3776901A

    公开(公告)日:1973-12-04

    申请号:US3776901D

    申请日:1968-04-01

    Inventor: KELLY K MATTHEWS J

    CPC classification number: C07D201/04

    Abstract: A METHOD FOR CONVERTING A KETOXIME TO AN N-SUBSTITUTED AMIDE BY REACTING A KETOXIME WITH A COMPLEX OF AN NSUBSTITUTED CARBOXYLIC ACID AMIDE AND SULFUR TRIOXIDE TO FORM A NOVEL COMPOUND OF THE KETOXIME, CARBOXYLIC ACID AMIDE AND SULFUR TRIOXIDE AND DECOMPOSING THIS COMPOUND TO PRODUCE AN N-SUBSTITUTED AMIDE CORRESPONDING TO THE KETOXIME. CYCLOHEXANONE OXIME IS CONVERTED TO CAPROLACTAM.

    Process for producing omega laurolactam
    176.
    发明授权
    Process for producing omega laurolactam 失效
    生产欧米茄乳液的方法

    公开(公告)号:US3767647A

    公开(公告)日:1973-10-23

    申请号:US3767647D

    申请日:1971-01-11

    CPC classification number: C07D201/04

    Abstract: A HIGH PURITY W-LAUROLACTAM IS PREPARED FROM A CRUDE CYCLODODECANONE OXIME CONTAINING 5% BY WEIGHT OR LESS OF CYCLODODECANONE BY SUBJECTING THE OXIME TO THE BECKMANN REARRANGEMENT REACTION IN THE PRESENCE OF SULFURIC ACID HAVING A CONCENTRATION OF 98% BY WEIGHT OR MORE OR FUMING SULFURIC ACID CONTAINING 20% BY WEIGHT OR LESS OF SULFURIC-ANHYDRIDE, SEPARATING THE THUS FORMED W-LAUROLACTAM FROM THE REACTION MIXTURE, DISSOLVING THE RESULTING W-LAUROLACTAM N A LIQUID AROMATIC HYDROCARBON, WASHING THE SOLUTION WITH AN ALKALI SOLUTION AT A TEMPERATURE OF 60* TO 120* C., AND RECOVERING W-LAUROLACTAM.

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