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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 10, 1980 - Issue 12
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Original Articles

Synthesis of 2-Nitrocyclopentanone

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Pages 929-932 | Published online: 05 Dec 2006
 

Abstract

The synthetic utility of cyclic α-nitroketones as well as the preparation of these useful synthetic intermediates has recently been reviewed1. Although the dipotassium salt of 2,5-dinitrocyclopentanone has been synthesized2, 2-nitrocyclopentanone itself could not be prepared by nitrating cyclopentanone with an alkyl nitrate and either potassium amide in liquid ammonia2 or potassium t-butoxide in tetrahydrofuran3. Furthermore, the reaction of 1-bromocyclopentene with dinitrogen tetroxide led only to a 15–20% yield of 2-nitrocyclopentanone as the 2,4-dinitrophenylhydrazone derivative4. The lone report of an actual preparation of 2-nitrocyclopentanone appears in a patent however with no characterization of the compound5. We now wish to report the synthesis and characterization of 2-nitrocyclopentanone, a potential versatile synthetic intermediate. Starting with cyclopentanone we have achieved the synthesis of the title compound by three methods outlined in Scheme I.

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