[CH:1]([C:4]1[O:8][C:7]([CH3:9])=[C:6]([C:10]([O:12]CC)=[O:11])[CH:5]=1)([CH3:3])[CH3:2]>[OH-].[Na+]>[CH:1]([C:4]1[O:8][C:7]([CH3:9])=[C:6]([C:10]([OH:12])=[O:11])[CH:5]=1)([CH3:3])[CH3:2]Saponification of 0.5 g of the ester was accomplished by refluxing 4 hours in 10 ml of 25% aqueous sodium hydroxide. Acidification precipitated the crude acid, which was recrystallized from water-ethanol to give 5isopropyl-2-methyl-3-furoic acid as white needles, mp 88.5° C.
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