| Beilstein Journal of Organic Chemistry | |
| Translation of microwave methodology to continuous flow for the efficient synthesis of diaryl ethers via a base-mediated SNAr reaction | |
| Charlotte Wiles1  Paul Watts2  | |
| [1] Chemtrix BV, Burgemeester Lemmensstraat 358, 6163 JT, Geleen, The Netherlands;Department of Chemistry, The University of Hull, Cottingham Road, Hull, HU6 7RX, UK; | |
| 关键词: automated synthesis; continuous flow; microreactor; microwave; nucleophilic substitution; organic bases; | |
| DOI : 10.3762/bjoc.7.160 | |
| 来源: DOAJ | |
【 摘 要 】
Whilst microwave heating has been widely demonstrated as a synthetically useful tool for rapid reaction screening, a microwave-absorbing solvent is often required in order to achieve efficient reactant heating. In comparison, microreactors can be readily heated and pressurised in order to “super-heat” the reaction mixture, meaning that microwave-transparent solvents can also be employed. To demonstrate the advantages associated with microreaction technology a series of SNAr reactions were performed under continuous flow by following previously developed microwave protocols as a starting point for the investigation. By this approach, an automated microreaction platform (Labtrix® S1) was employed for the continuous flow synthesis of diaryl ethers at 195 °C and 25 bar, affording a reduction in reaction time from tens of minutes to 60 s when compared with a stopped-flow microwave reactor.
【 授权许可】
Unknown