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    • 4. 发明申请
    • TECHNOLOGICAL METHOD FOR SYNTHESIS OF OPTICALLY PURE L-/D-LACTIDE CATALYZED BY BIOGENIC GUANIDINE
    • 用于生物活性剂催化的光学纯化的L- / D-乳酸的合成方法
    • US20160039782A1
    • 2016-02-11
    • US14782627
    • 2013-08-17
    • Nanjing University
    • Hong LiQuanxing ZhangNa ChengTianrong ZhangWei JiangWei HuangBingcai Pan
    • C07D319/12B01J31/02
    • C07D319/12B01J31/0208B01J31/0241B01J31/0271B01J2231/34
    • A technological method for synthesizing optically pure L-/D-lactide by using a biogenic guanidine catalysis method. The method of the present invention comprises: by using biogenic guanidine creatinine (CR) as a catalyst and L-/D-lactic acid (90% of mass content) as a raw material, synthesizing optically pure L-/D-lactide by using a reactive reduced pressure distillation catalysis method. The method of the present invention has advantages that the used catalyst is biogenic guanidine creatinine and free of toxicity, metal, and cytotoxicity; the synthesized lactide is high in optical purity (the specific rotation of the L-lactide [α]25 D=−276˜−280, and the specific rotation of the D-lactide [α]25 D=280), and does not contain any metal; the amount of the catalyst used in reaction is low, the technological process is simplified (a process for rectifying and purifying a crude lactide product by using a conventional method is avoided); and the technological method is simple and convenient to operate and easy in industrial implementation.
    • 通过生物胍胍催化方法合成光学纯的L- / D-丙交酯的技术方法。 本发明的方法包括:以生物胍胍肌酐(CR)为催化剂和L- / D-乳酸(90质量%)为原料,通过使用光学纯的L- / D-丙交酯 一种反应性减压蒸馏催化方法。 本发明的方法具有以下优点:所用催化剂是生物胍胍肌酐,无毒性,金属和细胞毒性; 合成的丙交酯的光学纯度高(L-丙交酯的比旋光度[α] 25 D = -276〜-280,D-丙交酯[α] 25 D = 280的比旋光度),不 含有任何金属; 反应中使用的催化剂的量低,简化了工艺过程(避免了通过常规方法对粗制丙交酯产物进行精馏和纯化的方法); 技术方法操作简便,工业实施方便。