Favorskii rearrangement
| Favorskii rearrangement | |
|---|---|
| Named after | Alexei Yevgrafovich Favorskii |
| Reaction type | Rearrangement reaction |
| Identifiers | |
| Organic Chemistry Portal | favorsky-reaction |
| RSC ontology ID | RXNO:0000385 |
In organic chemistry, the Favorskii rearrangement is a reaction of α-halo ketones with a nucleophilic base to acyl derivatives. In the rearrangement, the substrate extrudes the carbonyl carbon to a primary position, which then acylates the base. In the case of cyclic α-halo ketones, the Favorskii rearrangement constitutes a ring contraction: