1,2-Ethylene-bis(p-N2-phenylene-N1,N1-dimethylformamidine)
Institute of Macromolecular Chemistry "P.Poni", Gr. Ghica Voda Alley, 41 A, 6600, Iasi, Romania
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Molecules 2000, 5(7), M165; https://doi.org/10.3390/M165
Submission received: 16 May 2000
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Accepted: 2 June 2000
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Published: 10 July 2000
(This article belongs to the Section Molbank Section of Molecules, 1997-2001)
A mixture of 4.28 mmol (1.1328 g) bibenzil-4,4-di-yl-diisocyanate (1) [1] and 84 mmol (6.14 g) of redistilled N,N-dimethylformamide (2) was refluxed under stirring using a magnetically stirring-bar for 12 h, with complete absorption for any carbon dioxide in aqueous potassium hydroxide solution [2]. The major portion of the unchanged 2 was removed by vacuum distillation. After cooling the residue is triturated with diethyl ether. The precipitated solid is recrystallized from ethanol to afford 1.22 g (90 %) of 3.
M.p. : 182 - 183°C.
IR (cm-1): 1640; 1610 (C=N); 1510; 1500; 1370 (C-N); 840.
1H NMR (CDCl3): 7.5 (s, 2H, -CH=N); 6.95 (d, 4H, HAr, ortho to N=); 6.90 (d, 4H, HAr, ortho to -CH2-CH2-); 3.08 (s, 12 H, -CH3); 2.88 (s, 4H, >CH2).
Anal. calc. For C20H26N4 (322.457): C 74.50, H 8.13, N 17.37; Found: C 74.40, H 8.12, N 17.48.
References
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MDPI and ACS Style
Coseri, S.; Caraculacu, A.A. 1,2-Ethylene-bis(p-N2-phenylene-N1,N1-dimethylformamidine). Molecules 2000, 5, M165. https://doi.org/10.3390/M165
AMA Style
Coseri S, Caraculacu AA. 1,2-Ethylene-bis(p-N2-phenylene-N1,N1-dimethylformamidine). Molecules. 2000; 5(7):M165. https://doi.org/10.3390/M165
Chicago/Turabian StyleCoseri, Sergiu, and Adrian A. Caraculacu. 2000. "1,2-Ethylene-bis(p-N2-phenylene-N1,N1-dimethylformamidine)" Molecules 5, no. 7: M165. https://doi.org/10.3390/M165
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