Abstract

The asymmetric unit of the title compound, C7H3F4NO2, obtained as an inter­mediate in the synthesis of a coupling reagent, contains four independent and conformationally similar mol­ecules. The amine H atoms form both intra­molecular and inter­molecular N—H⋯Ocarbox­yl hydrogen bonds which, together with inter­molecular O—H⋯Ocarbox­yl hydrogen bonds and N—H⋯F associations form ribbon structures along the a axis.

Highlights

  • The asymmetric unit of the title compound, C7H3F4NO2, obtained as an intermediate in the synthesis of a coupling reagent, contains four independent and conformationally similar molecules

  • Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: ZS2117)

  • The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry

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Summary

Structure Reports Online

Key indicators: single-crystal X-ray study; T = 295 K; mean (C–C) = 0.005 A; R factor = 0.057; wR factor = 0.177; data-to-parameter ratio = 9.0. The asymmetric unit of the title compound, C7H3F4NO2, obtained as an intermediate in the synthesis of a coupling reagent, contains four independent and conformationally similar molecules. The amine H atoms form both intramolecular and intermolecular N—HÁ Á ÁOcarboxyl hydrogen bonds which, together with intermolecular O—HÁ Á ÁOcarboxyl hydrogen bonds and N—HÁ Á ÁF associations form ribbon structures along the a axis. Related literature The title compound was obtained as one of the intermediates in the synthesis of a coupling reagent (Xu et al, 2008; Liao et al, 2007), using the Hofmann rearrangement (Perumal & Muthialu, 2004) with 2-carboxyl-3,4,5,6-tetrafluorobenzamide (Cai et al, 1992)

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