Issue 11, 2012

Scope of direct arylation of fluorinated aromatics with aryl sulfonates

Abstract

The scope and limitations of direct arylation of fluorinated aromatics with aryl sulfonates was examined. Pd(OAc)2, in the presence of MePhos and KOAc in THF, efficiently catalyzed the direct arylation of fluoro aromatics with aryl triflates under ambient conditions. Sterically hindered triflates and heteroaryl triflates gave good to excellent yields of the cross coupled products using a modified catalyst system which involves Pd(OAc)2RuPhos at 100 °C. The direct arylation of electron deficient arenes with aryl mesylates is also established using Pd(OAc)2–SPhos as the catalyst in toluenetBuOH at 120 °C.

Graphical abstract: Scope of direct arylation of fluorinated aromatics with aryl sulfonates

Supplementary files

Article information

Article type
Paper
Submitted
02 Nov 2011
Accepted
16 Jan 2012
First published
17 Jan 2012

Org. Biomol. Chem., 2012,10, 2289-2299

Scope of direct arylation of fluorinated aromatics with aryl sulfonates

J. W. W. Chang, E. Y. Chia, C. L. L. Chai and J. Seayad, Org. Biomol. Chem., 2012, 10, 2289 DOI: 10.1039/C2OB06840K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements