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One pot synthesis of ethoxylated bisphenol A acrylate macro monomer from bisphenol A acrylate and ethylene oxide

机译:一种盆合成乙氧基化双酚A来自双酚A丙烯酸酯和环氧乙烯的丙烯酸酯宏观单体

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Ethoxylated bisphenol A acrylate, containing symmetric rigid aromatic rings and flexibility ethoxy groups, is a polyfunctional macro monomer. The homopolymer or copolymer well used as biomedical materials such as medical membrance, self-healing dental restorative formulation. To our knowledge, the monomer could be synthesized by either esterification of ethoxylated bisphenol A and acrylic acid or etherification of ethoxylated hydroxyethyl acrylate and bisphenol A. We developed a more atom economic route to produce the functional macro monomer. The inherent atom economy of the developed route is 100% which is much higher than that of the former multi-steps process. Catalysted by a heterogeneous acid-base bifunctional catalyst, ethylene oxide reacts with an active hydrogen free raw material, bisphenol A acrylate, to produce the target molecule. The inhibitors and some other reaction conditions were well discussed here. The conversion of bisphenol A acrylate was 90% at 140oC for 8 h with 1% wt catalyst and 0. 5% wt composite inhibitors in a steal autoclave.
机译:乙氧基化双酚A丙烯酸酯,含有对称刚性芳环和柔韧性乙氧基,是多官能宏观单体。均聚物或共聚物良好用作生物医学材料,如医用膜,自愈牙科修复化制剂。据我们所知,单体可以通过乙氧基化双酚A和丙烯酸丙烯酸的酯化或乙氧基化羟乙基乙酯醚化的酯化和双酚A醚合成。我们开发了更具原子的经济途径来生产功能宏观单体。发达路线的固有原子经济是100%,远高于前多步过程的型号。由非均相酸碱双官能催化剂催化,环氧乙烷与活性氢原料,双酚A丙烯酸酯反应,以产生靶分子。这里讨论了抑制剂和一些其他反应条件。双酚A丙烯酸酯的转化率为90%,在140℃下为8小时,1%wt催化剂和0.5%wt复合抑制剂在偷窃高压釜中。

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