Welcome to CEM.com

Optimizing Reactions in Nonpolar Solvents: A Microwave-Assisted Diels-Alder Reaction

September 3, 2019
Download File

Introduction

Microwave heating has been a versatile and powerful tool for synthetic chemists since the 1980s, advancing nanomaterial assembly, drug discovery, peptide synthesis, and more. The two mechanisms by which microwaves generate heat, ionic conduction and dipolar rotation, rely on an ion or molecule’s ability to align itself with the ever-oscillating electric field of a microwave. In general, highly polarized species undergo ionic conduction and dipolar rotation most readily, while low-polarity species are slowest to heat.

 


A common measure of polarity is the dielectric constant (ε’), which measures a compound’s ability to store electrical charges. Though useful, this value can sometimes contradict another important dielectric parameter, the dielectric loss constant (ε’’), which measures a solvent’s ability to dissipate absorbed microwave energy to its surroundings. In microwave heating, the dielectric loss constant (ε’’) provides the best gauge of a material’s ability to efficiently absorb microwaves and undergo heating. Typically, high-absorbing materials have an ε’ greater than 14, while low-absorbing solvents have an ε’’ less than 1 (Table 1).

 


A common misconception regarding microwave heating, however, is that microwaves can benefit only experiments employing polar solvent systems. The advantages of microwave heating can be harnessed despite the dielectric characteristics of a solvent; most reactions involve polar and/or ionic species that can interact directly and instantaneously with microwave energy, even if the solvent does not absorb effectively.

 


To demonstrate the efficacy of microwave heating in transformations employing low-polarity solvents, the simple modification and optimization of a Diels-Alder reaction in toluene (Scheme 1) was adapted from an established protocol employing water. This common cycloaddition is favored for its ability to produce ring structures and two new carbon-carbon bonds.

 

Table 1: The dielectric constants and dielectric loss constants of six common solvents

Solvent Dielectric Constant (ε') Dielectric Loss Constant (ε’’)
DMSO 45.0 37.125
Water 80.4 9.889
Acetonitrile 37.5 2.325
DCM 9.1 0.382
Toluene 2.4 0.096
Hexanes 1.9 0.038

 Microwave-heated Diels-Alder reaction in toluene

Scheme 1: Microwave-heated Diels-Alder reaction in toluene