Jamison, T. F. et al.: 2018 Science of Synthesis, 2018/5: Flow Chemistry in Organic Synthesis DOI: 10.1055/sos-SD-228-00262
Flow Chemistry in Organic Synthesis

15.3 Flow Chemistry in the Pharmaceutical Industry: Part 3

More Information

Book

Editors: Jamison, T. F.; Koch, G.

Authors: Beeler, A. B.; Beingessner, R. L.; Bottecchia, C.; Browne, D. L.; Coley, C. W.; Ferguson, S.; Folgueiras-Amador, A. A.; Gilmore, K.; Hicklin, R. W.; Imbrogno, J.; Itsuno, S.; Jamison, T. F.; Jensen, K. F.; Kelly, L. P.; Kerr, M. S.; Kiesman, W. F.; Kim, H.; Kwok, D.-I. A.; Ley, S. V.; Longstreet, A. R.; May, S. A.; McTeague, T. A.; Mijalis, A. J.; Mo, Y.; Moon, S.; Myerson, A.; Noël, T.; O’Brien, A. G.; O’Brien, M.; O’Mahony, M.; Opalka, S. M.; Pentelute, B. L.; Polyzos, A.; Schepartz, A.; Seeberger, P. H.; Seo, H.; Steinauer, A.; Stelzer, T.; Stephenson, C. R. J.; Strom, A. E.; Styduhar, E. D.; Sun, A. C.; Telmesani, R.; Thomas, D. A.; Tran, T. H.; Ullah, M. S.; Wicker, A. C.; Wirth, T.; Yoshida, J.

Title: Flow Chemistry in Organic Synthesis

Print ISBN: 9783132423312; Online ISBN: 9783132423350; Book DOI: 10.1055/b-006-161272

Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry

Science of Synthesis Reference Libraries



Parent publication

Title: Science of Synthesis

DOI: 10.1055/b-00000101

Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.

Type: Multivolume Edition

 


Abstract

When considering whether to develop a flow-chemistry approach to a particular synthetic route, the criteria of safety, quality, cost, sustainability, scalability, and speed are all considered. This chapter presents a case study of a single reaction, the formylation of an aryl bromide, being performed in a batch reactor, a microreactor, a plug-flow reactor, and a spinning-disk reactor. An assessment of the various technologies is made with respect to the abovementioned criteria.

 
  • 7 Kopach ME, Cole KP, Pollock PM, Johnson MD, Braden TM, Webster LP, McClary Groh J, McFarland AD, Schafer JP, Adler JJ, Rosemeyer M. Org. Process Res. Dev. 2016; 20: 1581
  • 9 Throughout this chapter, the terms butyllithium and BuLi refer to the unbranched alkyllithium, n-butyllithium.
  • 21 Roberge D, Rainone F, Quittmann W, Gottsponer M, Eyholzer M. WO 2011023761, 2011
  • 25 Boodhoo K, In: Process Intensification for Green Chemistry: Engineering Solutions for Sustainable Chemical Processing Boodhoo K, Harvey A. Wiley Hoboken, NJ 2013; 59-90
  • 27 A newer model can now operate at pressures of up to 10 bar.
  • 32 Poechlauer P, Colberg J, Fisher E, Jansen M, Johnson MD, Koenig SG, Lawler M, Laporte T, Manley J, Martin B, OʼKearney-McMullan A. Org. Process Res. Dev. 2013; 17: 1472
  • 36 May SA, Johnson MD, Braden TM, Calvin JR, Haeberle BD, Jines AR, Miller RD, Plocharczyk EF, Rener GA, Richey RN, Schmid CR, Vaid RK, Yu H. Org. Process Res. Dev. 2012; 16: 982
  • 39 Hohmann L, Löbnitz L, Menke C, Santhirakumaran B, Stier P, Stenger F, Dufour F, Wiese G, zur Horst-Meyer S, Kusserow B, Zang W, Nirschl H, Kockmann N. Chem. Eng. Technol. 2018; 41: 1152
  • 40 Cole KP, McClary Groh J, Johnson MD, Burcham CL, Campbell BM, Diseroad WD, Heller MR, Howell JR, Kallman NJ, Koenig TM, May SA, Miller RD, Mitchell D, Myers DP, Myers SS, Phillips JL, Polster CS, White TD, Cashman J, Hurley D, Moylan R, Sheehan P, Spencer RD, Desmond K, Desmond P, Gowran O. Science (Washington, D. C.) 2017; 356: 1144