Suzuki-Miyaura Coupling of (Hetero)Aryl Sulfones: Complementary Reactivity Enables Iterative Polyaryl Synthesis.

Paul Chatelain,Abhijit Sau,Joseph Moran,Christopher N. Rowley

doi:10.1002/anie.201908336

Abstract

Ideal organic syntheses involve the rapid construction of C-C bonds, with minimal use of functional group interconversions. The Suzuki-Miyaura cross-coupling (SMC) is a powerful way to form biaryl linkages, but the relatively similar reactivity of electrophilic partners makes iterative syntheses involving more than two sequential coupling events difficult to achieve without additional manipulations. Here we introduce (hetero)aryl sulfones as electrophilic coupling partners for the SMC reaction, which display an intermediate reactivity between those of typical aryl (pseudo)halides and nitroarenes. The new complementary reactivity allows for rapid sequential cross-coupling of arenes bearing chloride, sulfone and nitro leaving groups, affording non-symmetric ter- and quateraryls in only 2 or 3 steps, respectively. The SMC reactivity of (hetero)aryl sulfones is demonstrated in over 30 examples. Mechanistic experiments and DFT calculations are consistent with oxidative addition into the sulfone C-S bond as the turnover-limiting step. The further development of electrophilic cross-coupling partners with complementary reactivity may open new possibilities for divergent iterative synthesis starting from small pools of polyfunctionalized arenes.

Highlights

Ideal organic syntheses involve the rapid construction of CC bonds, with minimal use of functional group interconversions
We describe the discovery and development of the Suzuki-Miyaura cross-coupling (SMC) reaction ofaryl sulfones, which possess an intermediate level of reactivity between aryl chlorides and nitroarenes, allowing for rapid access to non-symmetric terand quateraryl compounds via iterative coupling sequences
When RuPhos was used as ligand in the presence of K3PO4, catalytic Pd(acac)2, and a small amount of DMSO, diphenyl sulfone underwent coupling with 4-methoxyphenylboronic acid at 130 °C

Summary

Introduction

Ideal organic syntheses involve the rapid construction of CC bonds, with minimal use of functional group interconversions. We describe the discovery and development of the SMC reaction of (hetero)aryl sulfones, which possess an intermediate level of reactivity between aryl chlorides and nitroarenes, allowing for rapid access to non-symmetric terand quateraryl compounds via iterative coupling sequences.

Results

Conclusion