Literature DB >> 27294205

Cross-Coupling Biarylation of Nitroaryl Chlorides Through High Speed Ball Milling.

Solita Lam1, Yvonne Puplampu-Dove1, Adrienne Morris1, Ayunna Epps1, Ghislain Mandouma1.   

Abstract

Solvent-free reaction using a high-speed ball milling technique has been applied to the classical Ullmann coupling reaction. Cross-coupling biarylation of several nitroaryl chlorides was achieved in good yields when performed in custom-made copper vials through continuous shaking without additional copper or solvent. Cross-coupling products were obtained almost pure and NMR-ready. These reactions were cleaner than solution phase coupling which require longer reaction time in high boiling solvents, and added catalysts as well as lengthy extraction and purification steps. Gram quantities of cross biaryl compounds have been synthesized with larger copper vials, a proof that this method can be used to reduce industrial waste and for sustainability.

Entities:  

Keywords:  Ball Milling; Biarylation; Cross-coupling; High Speed; Solvent-free Reaction; Ullmann

Year:  2015        PMID: 27294205      PMCID: PMC4902293     

Source DB:  PubMed          Journal:  Int J Innov Educ Res        ISSN: 2411-2933


  16 in total

1.  Aryl-aryl bond formation one century after the discovery of the Ullmann reaction.

Authors:  Jwanro Hassan; Marc Sévignon; Christel Gozzi; Emmanuelle Schulz; Marc Lemaire
Journal:  Chem Rev       Date:  2002-05       Impact factor: 60.622

2.  Formation of carbon--carbon bonds under catalysis by transition-metal nanoparticles.

Authors:  Marcial Moreno-Mañas; Roser Pleixats
Journal:  Acc Chem Res       Date:  2003-08       Impact factor: 22.384

3.  Direct coupling of pyrroles with carbonyl compounds: short enantioselective synthesis of (S)-ketorolac.

Authors:  Phil S Baran; Jeremy M Richter; David W Lin
Journal:  Angew Chem Int Ed Engl       Date:  2005-01-14       Impact factor: 15.336

Review 4.  Copper-mediated coupling reactions and their applications in natural products and designed biomolecules synthesis.

Authors:  Gwilherm Evano; Nicolas Blanchard; Mathieu Toumi
Journal:  Chem Rev       Date:  2008-08       Impact factor: 60.622

5.  Copper complexes of anionic nitrogen ligands in the amidation and imidation of aryl halides.

Authors:  Jesse W Tye; Zhiqiang Weng; Adam M Johns; Christopher D Incarvito; John F Hartwig
Journal:  J Am Chem Soc       Date:  2008-07-03       Impact factor: 15.419

6.  Catalytic C-C, C-N, and C-O Ullmann-type coupling reactions.

Authors:  Florian Monnier; Marc Taillefer
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

7.  Palladium and copper-catalysed arylation reactions in the presence of water, with a focus on carbon-heteroatom bond formation.

Authors:  Mónica Carril; Raul SanMartin; Esther Domínguez
Journal:  Chem Soc Rev       Date:  2008-01-08       Impact factor: 54.564

8.  Ball milling in organic synthesis: solutions and challenges.

Authors:  Achim Stolle; Tony Szuppa; Silke E S Leonhardt; Bernd Ondruschka
Journal:  Chem Soc Rev       Date:  2011-03-08       Impact factor: 54.564

9.  Carbon-carbon coupling reactions catalyzed by heterogeneous palladium catalysts.

Authors:  Lunxiang Yin; Jürgen Liebscher
Journal:  Chem Rev       Date:  2007-01       Impact factor: 60.622

10.  Design and evolution of copper apatite catalysts for N-arylation of heterocycles with chloro- and fluoroarenes.

Authors:  Boyapati M Choudary; Chidara Sridhar; Mannepalli L Kantam; Gopaldasu T Venkanna; Bojja Sreedhar
Journal:  J Am Chem Soc       Date:  2005-07-20       Impact factor: 15.419

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