Chemical Transformations of Tetracyclo[3.3.1.13,7.01,3]decane (1,3-Dehydroadamantane): VI. Reactions of 1,3-Dehydroadamantane with Carboxylic Acid Chlorides


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1,3-Dehydroadamantane reacted with saturated carboxylic acid chlorides to give the corresponding 1-acyl-3-chloroadmantanes as the major products. In some cases, minor products of insertion into the Cα–H bond of acyl chloride were formed. The reactions of 1,3-dehydroadamantane with aromatic (heteroaromatic) carboxylic acid chlorides selectively afforded aryl (hetaryl) 3-chloroadamantan-1-yl ketones. The described reactions provide a synthetic route to difficultly accessible alkyl (aryl) ketones containing a 3-chloroadamantan- 1-yl group in one step under mild conditions with high yields.

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V. Mokhov

Volgograd State Technical University

Email: butov@volpi.ru
俄罗斯联邦, pr. imeni Lenina 28, Volgograd, 400005

G. Butov

Volzhsky Polytechnic Institute (Branch)

编辑信件的主要联系方式.
Email: butov@volpi.ru
俄罗斯联邦, ul. Engel’sa 42a, Volzhsky, Volgograd oblast, 404121

K. Saad

Volzhsky Polytechnic Institute (Branch)

Email: butov@volpi.ru
俄罗斯联邦, ul. Engel’sa 42a, Volzhsky, Volgograd oblast, 404121

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