Abstract
The crystal structure of α-(N-benzoxazoline-2-one) acetic acid is studied in the following forms: hydrate, solvate with formic acid, organic monoethanolammonium salt (NН2(CH2)2OH) in two polymorphs produced by minor changes in the crystallization temperature, and also its ethylenediammonium salt (NН2(CH2)2NH2) in the 2:1 ratio, where amino groups participate in the deprotonation of two molecules of α-(N-benzoxazoline-2-one) acetic acid. Weak intermolecular hydrogen and dative bonds in the crystals consisting of different molecules are analyzed.
Similar content being viewed by others
References
Ch. S. Tang, H. Chang, D. Hoo, et al., Phytochemistry, 14, No. 9, 2077–2079 (1975).
E. Smissman, B. Lapidus, and D. Beck, J. Am. Chem. Soc., 79, No. 17, 4697–4699 (1957).
Ch. M. Chen and M. T. Chen, Phytochemistry, 15, No. 12, 1997–1999 (1976).
J. B. Bredenberg, E. Honkanen, and A. I. Virtanen, Acta Chem. Scand., 16, 135–141 (1962).
E. Honkanen and A. I. Virtanen, Acta Chem. Scand., 15, 221/222 (1961).
J. R. Geigy, Patent DE No. 1023627B (1960).
E. Model and J. Bindler, US Patent No. 9222794 (1960).
V. G. Blinova, L. G. Sidorina, S. N. Ivanova, et al., Abstr. J. Chem., 4Zh289Dep (1974).
CrysAlisPro. Version 1.171.33.40, Oxford Diffraction, UK (2007).
G. M. Sheldrick, Acta Crystallogr., A46, 467–473 (1990).
G. M. Sheldrick, SHELXL-97. Program for the Refinement of Crystal Structures, University of Göttingen, Germany (1997).
Siemens. XP. Molecular Graphics Program. Version 5.03, Siemens Analytical X-ray Instruments Inc., Madison, Wisconsin, USA (1994).
Author information
Authors and Affiliations
Additional information
Original Russian Text © 2015 J. M. Ashurov, N. S. Mukhamedov, B. Tashkhodzhaev, B. T. Ibragimov.
Translated from Zhurnal Strukturnoi Khimii, Vol. 56, No. 6, pp. 1201–1207, November–December, 2015.
Rights and permissions
About this article
Cite this article
Ashurov, J.M., Mukhamedov, N.S., Tashkhodzhaev, B. et al. Crystal structure of α-(N-benzoxazoline-2-one) acetic acid hydrate, solvate, and salts. J Struct Chem 56, 1148–1153 (2015). https://doi.org/10.1134/S0022476615060190
Received:
Revised:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S0022476615060190