Improved Synthesis of and Nucleophilic Addition to 2-Formyl-2-Cyclohexenone

Tetrahedron Lett. 2015 Jan 8;56(2):386-389. doi: 10.1016/j.tetlet.2014.11.100.

Abstract

A preparation of 2-formyl-2-cyclohexenone in nearly quantitative yield and purity of approximately 95% is described. It is scalable and has been extended to the synthesis of the 5- and 7-membered ring homologs with comparable yields. Conditions have also been developed for the successful conjugate addition of dimethylmalonate to 2-formyl-2-cyclohexenone, in good and scalable yield (60%). This result has been extended to 5 other nucleophile classes, and the dimethylmalonate conjugate addition has been demonstrated with 2-formyl-2-cyclopentenone and 2-formyl-2-cycloheptenone.

Keywords: 2-formyl-2-cycloalkenone; 2-formyl-2-cyclohexenone; Michael Addition; conjugate addition; dimethylmalonate.