Synfacts 2015; 11(4): 0441
DOI: 10.1055/s-0034-1380492
Polymer-Supported Synthesis
© Georg Thieme Verlag Stuttgart · New York

Flow-Generated Diazo Compounds and Their Use in Cross-Coupling

Contributor(s):
Yasuhiro Uozumi
,
Yoichi M. A. Yamada
,
Heeyoel Baek
Tran DN, Battilocchio C, Lou S.-B, Hawkins JM, Ley SV * University of Cambridge, UK; Pfizer Worldwide Research and Development, Groton, USA
Flow Chemistry as a Discovery Tool to Access sp2–sp3 Cross-Coupling Reactions via Diazo Compounds.

Chem. Sci. 2015;
6: 1120-1125
Further Information

Publication History

Publication Date:
18 March 2015 (online)

 

Significance

Unstable diazo compounds were generated as reactive intermediates in a flow system using a MnO2-packed cartridge with Hünig’s base. The resulting diazo compounds reacted with carboxylic acids and arylboronic acids under flow conditions to give the corresponding esters 2af in 72–100% yield and the C–C coupling products 3af in 67–95% yield, respectively.


#

Comment

The generated diazo compounds were detected and titrated by in-line IR spectroscopy. The MnO2-packed cartridge was regenerated by flowing tert-butyl hydroperoxide in dichloromethane and reused twice with a slight loss of activity.


#
#