| 1.08 g/cm³|
Hagemann's ester, or ethyl-2-methyl-4-oxo-2-cyclohexenecarboxylate, is an organic compound that was first prepared and described in 1893 by German chemist Carl Hagemann. The compound is used in organic chemistry as a reagent in the synthesis of many important natural products including sterols, trisporic acids, and terpenoids.
Hagemann's ester Wikipedia
Methylene iodide and two equivalents of acetoacetic ester react in the presence of sodium methoxide to form the diethyl ester of 2,4-diacetyl pentane. This precursor is treated with base to induce cyclization. Finally, heat is applied to generate Hagemann's ester.
Soon after Hagemann, Knovenagel presented the following modified procedure. Formaldehyde and two equivalents of acetoacetic ester undergo condensation in the presence of catalytic piperidine to produce the diethyl ester of 2,4-diacetyl pentane. This precursor is treated with base to induce cyclization. Finally, heat is applied to generate Hagemann's ester.
2-Methoxy-1,3-butadiene and ethyl-2-butynoate undergo a Diels Alder reaction to generate a precursor. The precursor is hydrolyzed to obtain Hagemann's ester. By varying the substituents on the butynoate starting material, this approach allows for different C2 alkylated Hagemann's ester derivatives to be synthesized.
Methyl vinyl ketone, acetoacetic ester, and diethyl-methyl-(3-oxo-butyl)-ammonium iodide react to form a cyclic aldol product. Sodium methoxide is added to generate Hagemann's ester.
Methyl vinyl ketone and acetoacetic ester undergo aldol cyclization in the presence of catalytic pyrrolidinum acetate or Triton B or sodium ethoxide to produce Hagemann's ester.