Starting with methyl propanoate, how could you prepare 4-methyl- 3-heptanone? Because the starting material is an ester and the target molecule has more carbons than the starting material, a Claisen condensation appears to be a good way to start this synthesis. The Claisen condensation forms a β-keto ester that then can be easily alkylated at the desired carbon because it is flanked by two carbonyl groups. Acid-catalyzed hydrolysis will form a 3 -oxocarboxylic acid that will decarboxylate when h
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