化工学报 ›› 2019, Vol. 70 ›› Issue (8): 3202-3209.DOI: 10.11949/0438-1157.20190189

• • 上一篇    

用微反应器实现可见光驱动的不对称氧化连续化反应

冯世豪1(),唐晓飞1,都健2,孟庆伟1()   

  1. 1. 大连理工大学化工学院, 精细化工国家重点实验室,辽宁 大连 116024
    2. 大连理工大学化工系统工程研究所,辽宁 大连 116024
  • 收稿日期:2019-03-05 修回日期:2019-05-13 出版日期:2019-08-05 发布日期:2019-08-05
  • 通讯作者: 孟庆伟
  • 作者简介:冯世豪(1994—),男,硕士研究生,<email>liwupu000@126.com</email>
  • 基金资助:
    国家自然科学基金项目(21476041)

Asymmetric continuous oxidation in microreactor driven by visible light

Shihao FENG1(),Xiaofei TANG1,Jian DU2,Qingwei MENG1()   

  1. 1. State Key Laboratory of Fine Chemicals, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, Liaoning, China
    2. Institute of Process Systems Engineering, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, Liaoning, China
  • Received:2019-03-05 Revised:2019-05-13 Online:2019-08-05 Published:2019-08-05
  • Contact: Qingwei MENG

摘要:

将可见光催化、不对称合成、分子氧氧化和连续化集成,创新性地用玻璃微通道反应器实现可见光活化分子氧氧化的β-酮酸酯类化合物的不对称α-羟基化反应的连续工艺。用金鸡纳碱衍生的相转移有机催化剂在气-液-液多相体系内实现可见光催化,分子氧不对称氧化连续反应。在心形微通道反应器内,1-茚酮-2-甲酸金刚酯底物完全氧化为(S)-2-羟基-1-茚酮-2-甲酸金刚酯,产物收率95%,对映选择性87.0%。与间歇反应相比,采用微反应器的连续反应在保持产物高立体选择性基础上将30 min反应停留时间缩短至1.08 min。该方法具有快速、低能耗、连续、高效等优势,具有良好的工业化前景。

关键词: 光化学, 不对称有机催化, 分子氧氧化, 多相反应, 分子合成, 微反应器

Abstract:

Photocatalysis, asymmetric synthesis and molecular oxygen oxidation are combined with continuous reaction. Using a glass microreactor, a continuous reaction for asymmetric α-hydroxylation of β-keto ester compound is oxidized by 1O2 under visible light. The reaction is catalyzed by cinchona alkaloid phase transfer catalyst in gas-liquid-liquid heterogeneous system. The desired product is obtained in high yield (95%) and good enantio selectivity (87.0%) in microreactor. Compared with the batch reaction, continuous reaction greatly reduces reaction residence time from 30 min to 1.08 min and maintains high stereo selectivity. The method has the advantages of fast, low energy consumption, continuous and high efficiency, and has good industrialization prospects.

Key words: photochemistry, asymmetric organic catalysis, molecular oxygen oxidation, heterogeneous reaction, molecular synthesis, microreactor

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