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Chemistry for Sustainable Development

2022 year, number 6

Optimization of the Synthesis of 2-Adamantanecarboxylic Acid

A. A. MUNKUEV1, A. ZH. SHESHKOVAS2, E. V. SUSLOV1, K. P. VOLCHO1, N. F. SALAKHUTDINOV1
1Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia
2Novosibirsk State University, Novosibirsk, Russia
Keywords: adamantane, biological activity, Corey-Chaykovsky reaction
Pages: 612-616

Abstract

To date, compounds having an adamantane moiety have found wide application in the pharmaceutical industry. Despite the fact that most biologically active adamantyl-bearing derivatives contain substituents in the first position of the adamantane molecule, some derivatives with substituents in the second position have also shown valuable pharmacological properties. While 1-adamantanecarboxylic acid is an inexpensive and commercially available reagent, its 2-substituted analogue is substantially less available, and therefore, the development and optimization of approaches to the synthesis of 2-adamantanecarboxylic acid are of great importance. In this work, a three-stage method for the synthesis of 2-adamantanecarboxylic acid has been optimized, based on the Corey-Chaykovsky reaction of 2-adamantanone with trimethylsulphoxonium iodide in the presence of potassium hydroxide, followed by acid-catalyzed opening of the oxirane ring and oxidation of aldehyde 9 to the target carboxylic acid. The total yield of the target product is 70 %.