Abstract

The title compound, C10H11N3O2, was synthesized by the reaction of 1H-benzotriazole with ethyl 2-chloro­acetate in ethanol. The non-H atoms, excluding the benzotriazol-1-yl group, are almost coplanar (r.m.s. deviation of the non-H atoms = 0.0409 Å). The dihedral angle formed between this plane and the benzotriazole ring is 79.12 (5)° In the crystal, weak inter­molecular C—H⋯N and C—H⋯O inter­actions help to consolidate the three-dimensional network.

Highlights

  • The title compound, C10H11N3O2, was synthesized by the reaction of 1H-benzotriazole with ethyl 2-chloroacetate in ethanol

  • The dihedral angle formed between this plane and the benzotriazole ring is 79.12 (5) In the crystal, weak intermolecular C—HÁ Á ÁN and C—HÁ Á ÁO interactions help to consolidate the three-dimensional network

  • Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: VM2062)

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Summary

Structure Reports Online

Key indicators: single-crystal X-ray study; T = 296 K; mean (C–C) = 0.004 A; R factor = 0.067; wR factor = 0.231; data-to-parameter ratio = 18.6. The title compound, C10H11N3O2, was synthesized by the reaction of 1H-benzotriazole with ethyl 2-chloroacetate in ethanol. The non-H atoms, excluding the benzotriazol-1-yl group, are almost coplanar (r.m.s. deviation of the non-H atoms = 0.0409 A ). The dihedral angle formed between this plane and the benzotriazole ring is 79.12 (5) In the crystal, weak intermolecular C—HÁ Á ÁN and C—HÁ Á ÁO interactions help to consolidate the three-dimensional network. Related literature For related structures, see: Shi et al (2007a,b); Ji et al (2008); Zhang et al (2009)

Bruker SMART APEX CCD diffractometer
DÁ Á ÁA
Crystal data
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