Issue 7, 2014

Sulfur–silicon bond activation catalysed by Cl/Br ions: waste-free synthesis of unsymmetrical thioethers by replacing fluoride catalysis and fluorinated substrates in SNAr reactions

Abstract

In contrast to conventional activation of Nu–SiR3 reagents by F ion attributed to the strong affinity of Si to F, S–Si activation can now be achieved using Cl/Br ions of TBAX as catalysts via formation of weaker X–Si bonds and Me3Si–X. This led to a waste-free synthesis of unsymmetrical thioethers via F-free SNAr reactions of activated (hetero)aryl halides and RS–SiMe3, with recovery of the useful Me3Si–X reagent in high yields.

Graphical abstract: Sulfur–silicon bond activation catalysed by Cl/Br ions: waste-free synthesis of unsymmetrical thioethers by replacing fluoride catalysis and fluorinated substrates in SNAr reactions

Supplementary files

Article information

Article type
Communication
Submitted
26 Mar 2014
Accepted
19 May 2014
First published
19 May 2014

Green Chem., 2014,16, 3444-3449

Sulfur–silicon bond activation catalysed by Cl/Br ions: waste-free synthesis of unsymmetrical thioethers by replacing fluoride catalysis and fluorinated substrates in SNAr reactions

X. Jia, L. Yu, J. Liu, Q. Xu, M. Sickert, L. Chen and M. Lautens, Green Chem., 2014, 16, 3444 DOI: 10.1039/C4GC00535J

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