74384-41-1Relevant academic research and scientific papers
Fries Rearrangement of ortho- and para-Methoxy Phenyl Acetates. The formation of Ketoesters
Martin, Robert,Gros, Nicole,Boehmer, Volker,Kaemmerer, Hermann
, p. 81 - 92 (2007/10/02)
During the Fries rearrangement of o- and p-methoxy phenyl acetates with AlCl3 in nitromethane at 20 deg C substitution occurs mainly in the p-position of the phenolic residue to yield p-acylphenols.Larger quantities of o-acylphenols are obtained only, if
