In the title compound, C9H15NO·C 6H2Cl2O4 [sytematic name: 2-azaspiro-[4.5]decan-3-onechloranilic acid (1/1)], the cyclo-hexane ring of the lactam molecule adopts a slightly distorted normal chair conformation and the five-membered 3-azaspiro ring is in a slightly distorted chair conformation. The dihedral angle between the least-squares planes of the cyclohexane and 3-azaspiro rings is 84.0 (3)°. In the crystal, the chloranilic acid mol-ecule and the gabapentin-lactum mol-ecules are held together by strong inter-molecular N-H⋯O and O-H⋯O hydrogen bonds with two bifurcated O acceptor atoms on the chloranilic acid mol-ecule and one on the gabapentin-lactum mol-ecule, each bonding with an inter-and intra-molecular hydrogen bond. The molecules are linked into chains parallel to (011) and propagating along the b axis.
CITATION STYLE
Jasinski, J. P., Butcher, R. J., Hakim Al-Arique, Q. N. M., Yathirajan, H. S., & Narayana, B. (2010). Gabapentin-lactumchloranilic acid (1/1). Acta Crystallographica Section E: Structure Reports Online, 66(1). https://doi.org/10.1107/S1600536809053410
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