Abstract
This paper describes our efforts in proposing a novel mechanism for the
formation of the major degradant of clobetasol propionate under weakly acidic
conditions through a comprehensive investigation. In the proposed mechanism, the
key Favorskii intermediate plays a critical role. This variation of the
original Favorskii rearrangement, which proceeds only under alkaline conditions, has
not been reported before. This mechanism enriches the understanding of
the degradation chemistry of corticosteroids containing the α-haloketone
moiety on their 17-position.