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19 sie 2024 · 2, 4, 6-Tribromoaniline Principle. Aniline undergoes nucleophilic substitution with bromine, even in cold. The bromine atoms enter at the two ortho positions and the para position with the formation of 2,4,6-tribromoaniline.
2,4,6-Tribromoaniline Compound with spectra: 14 NMR, 4 FTIR, 1 Raman, and 8 MS (GC)
Principle: Aniline undergoes nucleophilic substitution with bromine, The bromine atoms enter at the two ortho positions and the para position with the format...
The document describes the preparation of 2,4,6-tribromoaniline from aniline via electrophilic aromatic substitution. Aniline undergoes bromination at the ortho and para positions due to the activating effect of the amino group. This results in 2,4,6-tribromoaniline.
2,4,6-Tribromoaniline UNII 0C2N8WIL3B Molecular formula C 6 H 4 Br 3 N Molecular weight 329.82 Percent composition C 21.85%, H 1.22%, Br 72.68%, N 4.25% Standard InChI InChI=1S/C6H4Br3N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2 Standard InChIKey GVPODVKBTHCGFU-UHFFFAOYSA-N
2,4,6-Tribromoaniline can be prepared by treating bromine water with aniline in a solution of acetic acid or dilute hydrochloric acid: By reacting bromine with aniline in water, a white precipitate immediately forms and that is 2,4,6-tribromoaniline.
5 maj 2023 · Abstract. In this study, the 2,4,6-Tribromoaniline is synthesized from aniline and bromine by halogenation (bromination) reaction. The presented study comprises synthesis, solubility testing,...
