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5-碘-3-苯基-2,1-苯并恶唑。

5-Iodo-3-phenyl-2,1-benzoxazole.

作者信息

Teslenko Yuriy, Matiychuk Vasyl S, Kinzhybalo Vasyl, Lis Tadeusz, Obushak Mykola D

机构信息

Department of Organic Chemistry, Ivan Franko National University of Lviv, Kyryla and Mefodiya 6, Lviv 79005, Ukraine.

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2013 Mar 9;69(Pt 4):o508. doi: 10.1107/S1600536813005862. Print 2013 Apr 1.

DOI:10.1107/S1600536813005862
PMID:23634055
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3629537/
Abstract

The title compound, C13H8INO, was prepared by a condensation reaction of 4-nitro-benzene with phenyl-acetonitrile in NaOH-ethanol solution. There are two independent mol-ecules in the asymmetric unit, in which the dihedral angles between the benzene ring and the benzoisoxazole unit are 4.2 (3) and 4.1 (3)°. The crystal packing is governed by C-H⋯N, C-I⋯π and C-I⋯O inter-actions.

摘要

标题化合物C₁₃H₈INO是通过4-硝基苯与苯乙腈在氢氧化钠-乙醇溶液中发生缩合反应制备的。不对称单元中有两个独立的分子,其中苯环与苯并异恶唑单元之间的二面角分别为4.2(3)°和4.1(3)°。晶体堆积由C-H⋯N、C-I⋯π和C-I⋯O相互作用控制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e82/3629537/9096b90931a8/e-69-0o508-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e82/3629537/d408f324ab77/e-69-0o508-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e82/3629537/9096b90931a8/e-69-0o508-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e82/3629537/d408f324ab77/e-69-0o508-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e82/3629537/9096b90931a8/e-69-0o508-fig2.jpg

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