Abstract
A wide variety of 2′-hydroxypolymethoxyacetophenones and propiophenones, e.g. 1a and 1b are used in the synthesis of flavone and ehromone natural products.1 Repeated attempts to prepare 1a and 1b by reacting 1,2,3,5-tetramethoxybenzene 2 with acetyl or propionyl chlorides and AlCl3 in ether2 gave products which were difficult to purify.3 We traced the problem to ring-ethoxy contaminants which were isolated and tentatively identified as 3a and 3b.