33539-21-8Relevant academic research and scientific papers
A New and Facile Iodine(III)-Mediated Approach for the Regioselective Alkoxylation of 2,5-Dihydroxyacetophenone
Prakash, Om,Pundeer, Rashmi,Kaur, Harpreet
, p. 2768 - 2770 (2007/10/03)
Oxidation of 2,5-dihydroxyacetophenone with iodobenzene diacetate (IBD) in different alcohols leads to regioselective alkoxylation, thereby providing a new and convenient route for the synthesis of 6-alkoxy-2,5- dihydroxyacetophenones.
Copper-catalysed oxidative alkoxylation of acyl- and carbomethoxy-hydroquinones
Capdevielle, Patrice,Maumy, Michel
, p. 379 - 384 (2007/10/03)
Oxidation of title hydroquinones by an [O2/CuICl] system in the presence of alcohols yields (71-88%) corresponding regioselectively 3-alkoxylated compounds. Compared with the classical procedure (silver oxide oxidation) in which alcohols have to be added to intermediate quinones in a second step, leading to a 1:1 mixture of starting material and final quinones, this new selective one-pot system does not oxidize alcohols and regenerates intermediate quinones from starting hydroquinones. Moreover, in situ trapping of the unstable formyl-quinone now allows the preparation of its 3-alkoxy derivative.
