Abstract
Symmetrical diaryl ketones were prepared by a cross-coupling reaction between aryl bromides and ethyl chloroformate. This new method, which uses a catalyst composed of CoBr2and a bipyridine ligand along with readily available starting materials, allows for the synthesis of a variety of symmetrical diaryl ketones in moderate to excellent yields (37–99 %) under mild conditions. This reaction, in which ethyl chloroformate acts as a surrogate of carbon monoxide in the presence of cobalt and zinc, represents an interesting alternative to previously known approaches for the synthesis of diarylmethanones.
| Original language | English |
|---|---|
| Pages (from-to) | 4554-4560 |
| Number of pages | 7 |
| Journal | European Journal of Organic Chemistry |
| Volume | 2016 |
| Issue number | 26 |
| DOIs | |
| Publication status | Published - 1 Sept 2016 |
| Externally published | Yes |
Keywords
- Cobalt
- Cross-coupling
- Homogeneous catalysis
- Synthetic methods
- Zinc