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20.5.1.7.9.2 Method 2: Ring Opening under Acidic Conditions

DOI: 10.1055/sos-SD-020-00774

Zhang, M.; Hanson, P. R.Science of Synthesis, (200720912.

The traditional approach to transform a lactone, e.g. 197 or 201, into the corresponding hydroxy ester is to react it with an alcohol in the presence of an acid, e.g. sulfuric ­acid[‌259‌‌261‌] or 4-toluenesulfonic acid (Scheme 61).[‌262‌‌264‌] Storage of alcoholic solutions of lactones, e.g. 198 or 200, on Amberlyst-15 also results in the formation of the corresponding hydroxy esters, e.g. 199, in high yields (Scheme 61).[‌265‌]

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