The Continuous-Flow Synthesis of Ibuprofen

被引:221
作者
Bogdan, Andrew R. [2 ]
Poe, Sarah L. [2 ]
Kubis, Daniel C. [2 ]
Broadwater, Steven J. [2 ]
McQuade, D. Tyler [1 ]
机构
[1] Florida State Univ, Chem Sci Lab, Dept Chem & Biochem, Tallahassee, FL 32306 USA
[2] Cornell Univ, Baker Lab, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
continuous processing; flow chemistry; microreactors; reactor design; synthetic methods; ORGANIC-SYNTHESIS; MULTISTEP SYNTHESIS; COUPLING REACTIONS; REACTORS; CHEMISTRY; MECHANISM; CATALYSIS; ACYLATION;
D O I
10.1002/anie.200903055
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Let relief flow forth I A three-step, continuous-flow synthesis of ibuprofen was accomplished using a simplified microreactor. By designing a synthesis in which excess reagents and byproducts are compatible with downstream reactions, no intermediate purification or isolation steps are required. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:8547 / 8550
页数:4
相关论文
共 47 条
  • [21] Organic synthesis using polymer-supported reagents, catalysts and scavengers in simple laboratory flow systems
    Hodge, P
    [J]. CURRENT OPINION IN CHEMICAL BIOLOGY, 2003, 7 (03) : 362 - 373
  • [22] A microcapillary flow disc reactor for organic synthesis
    Hornung, Christian H.
    Mackley, Malcolm R.
    Baxendale, Ian R.
    Ley, Steven V.
    [J]. ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2007, 11 (03) : 399 - 405
  • [23] Continuous flow techniques in organic synthesis
    Jas, G
    Kirschning, A
    [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2003, 9 (23) : 5708 - 5723
  • [24] Kirschning A, 2001, ANGEW CHEM INT EDIT, V40, P650, DOI 10.1002/1521-3773(20010216)40:4<650::AID-ANIE6500>3.3.CO
  • [25] 2-3
  • [26] KIRSCHNING A, 2001, ANGEW CHEM, V113, P670
  • [27] Greener approaches to organic synthesis using microreactor technology
    Mason, Brian P.
    Price, Kristin E.
    Steinbacher, Jeremy L.
    Bogdan, Andrew R.
    McQuade, D. Tyler
    [J]. CHEMICAL REVIEWS, 2007, 107 (06) : 2300 - 2318
  • [28] Rapid formation of amides via carbonylative coupling reactions using a microfluidic device
    Miller, PW
    Long, NJ
    de Mello, AJ
    Vilar, R
    Passchier, J
    Gee, A
    [J]. CHEMICAL COMMUNICATIONS, 2006, (05) : 546 - 548
  • [29] Selective monolithiation of dibromobiaryls using microflow systems
    Nagaki, Aiichiro
    Takabayashi, Naofumi
    Tomida, Yutaka
    Yoshida, Jun-ichi
    [J]. ORGANIC LETTERS, 2008, 10 (18) : 3937 - 3940
  • [30] Aryllithium compounds bearing alkoxycarbonyl groups: Generation and reactions using a microflow system
    Nagaki, Aiichiro
    Kim, Heejin
    Yoshida, Jun-ichi
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (41) : 7833 - 7836