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    • 10. 发明授权
    • Method for producing butyrolactones
    • 丁内酯的制备方法
    • US06346629B1
    • 2002-02-12
    • US09700426
    • 2000-11-15
    • Melanie BrunnerRalf-Thomas RahnUdo RheudeJochem Henkelmann
    • Melanie BrunnerRalf-Thomas RahnUdo RheudeJochem Henkelmann
    • C07D30702
    • C07D315/00
    • Process for producing butyrolactones of the general formula I where R1 and R2 are each hydrogen, alkyl, hydroxyalkyl, substituted or unsubstituted aryl or substituted or unsubstituted trialkylsilyl, by reacting alkynes of the general formula II where R1 and R2 are each as defined above, with carbon monoxide and water in the presence of a rhodium catalyst under pressures from 20 to 300 bar and hydrogenating the unhydrogenated 2(5H)-furanone intermediates comprises a) reacting the carbonylation reaction mixture with hydrogen at from 150 to 250° C. and from 100 to 300 bar, b) removing the precipitated catalyst and returning it into the carbonylation reaction, and c) subjecting the catalyst-free reaction mixture to a distillation to recover the butyrolactone.
    • 制备通式I的丁内酯的方法,其中R 1和R 2各自为氢,烷基,羟基烷基,取代或未取代的芳基或取代或未取代的三烷基甲硅烷基,其中通式II的炔烃其中R 1和R 2各自如上所定义,与一氧化碳 和铑催化剂存在下的水,在20-300巴的压力下氢化未氢化的2(5H) - 呋喃酮中间体包括:a)使羰基化反应混合物与氢在150-250℃和100-300巴条件下反应 ,b)除去沉淀的催化剂并将其返回到羰基化反应中,和c)使无催化剂反应混合物进行蒸馏以回收丁内酯。