REACTIONS OF 1-NITROCYCLOHEXENE
2305
14. Lyssenko, K.A., Korlyukov, A.A., and Antipin M.Yu.,
of ethanol–water mixture (1:1). The reaction mixture
was cooled to room temperature and kept for 24 h. The
precipitate was filtered off and dried in air. Yield
0.71 g (24%), mp 204–206°С (benzene). IR spectrum,
ν, cm–1 (KBr): 1595 (С=С), 1617 (С=N), 3340 (NH).
1Н NMR spectrum (DMSO-d6), δ, ppm: 1.70 m (6Н,
С4Н2, С5Н2, С6Н2), 2.27 m (2Н, С7Н2), 6.65 m, 7.03–
7.48 m (10Н, Ph), 7.76 s (1Н, NH). Found, %: С
79.08; H 6.67; N 14.52. C19H19N3. Calculated, %: C
78.86; H 6.62; N 14.52.
Mendeleev. Commun., 2005, p. 90.
15. Lyssenko, K.A., Korlyukov, A.A., Golovanov, D.G.,
Ketkov, S.Yu., and Antipin, M.Yu., J. Phys. Chem. A,
2006, vol. 110, p. 6545.
16. Lyssenko, K.A., Barzilovich, P.Yu., Nelyubina, Yu.V.,
Astafiev, E.A., Antipin, M.Yu., and Aldoshin, S.M., Izv.
Ross. Akad. Nauk, Ser. Khim., 2009, no. 1, p. 31.
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18. Sheldrick, G.M. SHELXTL v. 5.10, Structure
Determination Software Suit, Bruker AXS: Madison,
Wisconsin, USA.
ACKNOWLEDGMENTS
This work was financially supported by the Russian
Foundation for Basic Research (project no. 10-03-
00578-а) and by the President of Russian Federation
(grant no. MD-237.2010.3).
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RUSSIAN JOURNAL OF GENERAL CHEMISTRY Vol. 80 No. 11 2010