Reaction of 4,6-di-tert-butyl-3-nitrocyclohex-3,5-diene1,2-dione with secondary amines
- Authors: Ivakhnenko E.P.1, Malay V.I.1, Demidov O.P.2, Minkin V.I.1
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Affiliations:
- Institute of Physical and Organic Chemistry, Southern Federal University
- North Caucasus Federal University
- Issue: Vol 59, No 8 (2023)
- Pages: 1032-1040
- Section: Articles
- URL: https://journals.rcsi.science/0514-7492/article/view/141669
- DOI: https://doi.org/10.31857/S0514749223080049
- EDN: https://elibrary.ru/JPETEW
- ID: 141669
Cite item
Abstract
Reaction of 4,6-di- tert -butyl-3-nitrocyclohexa-3,5-diene-1,2-dione with secondary amines (piperidine, morpholine, 1-methylpiperazine) in isopropanol leads to a mixture of products formed as a result of parallel reactions of Michael addition and ANRORC. The compounds obtained were characterized by 1H NMR, 13C NMR, IR spectroscopy, and elemental analysis. Molecular structure of 3-nitrocyclohexa-3-ene-1,2-dione and cyclopenta1,3-diene derivatives was established by X-ray diffraction analysis.
Keywords
About the authors
E. P. Ivakhnenko
Institute of Physical and Organic Chemistry, Southern Federal University
Email: ivakhnenko@sfedu.ru
V. I. Malay
Institute of Physical and Organic Chemistry, Southern Federal University
O. P. Demidov
North Caucasus Federal University
Email: odemidov@gmail.com
V. I. Minkin
Institute of Physical and Organic Chemistry, Southern Federal University
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