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N1-(5-Fluoro-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine
Publication type: Journal Article
Publication date: 2017-12-02
DOI:
10.3390/m967
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Abstract
Treating 1,5-difluoro-2,4-dinitrobenzene (1) with N1-phenyl-5-(trifluoromethyl)benzene-1,2-diamine (4) and N,N-diisopropylethylamine in EtOH at ca. 0 °C for 4 h affords a mixture of N1-(5-ethoxy-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine (5) (38%) and N1-(5-fluoro-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine (6) (51%) that can be separated by chromatography. Repeating the reaction in dichloromethane led to the sole formation of N1-(5-fluoro-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine (6) in 96% yield.
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Zissimou G. A., Koutentis P. A. N1-(5-Fluoro-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine // MolBank. 2017. Vol. 2017. No. 4. p. M967.
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Zissimou G. A., Koutentis P. A. N1-(5-Fluoro-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine // MolBank. 2017. Vol. 2017. No. 4. p. M967.
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TY - JOUR
DO - 10.3390/m967
UR - https://doi.org/10.3390/m967
TI - N1-(5-Fluoro-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine
T2 - MolBank
AU - Zissimou, Georgia A.
AU - Koutentis, Panayiotis A.
PY - 2017
DA - 2017/12/02
PB - MDPI
SP - M967
IS - 4
VL - 2017
SN - 1422-8599
ER -
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@article{2017_Zissimou,
author = {Georgia A. Zissimou and Panayiotis A. Koutentis},
title = {N1-(5-Fluoro-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine},
journal = {MolBank},
year = {2017},
volume = {2017},
publisher = {MDPI},
month = {dec},
url = {https://doi.org/10.3390/m967},
number = {4},
pages = {M967},
doi = {10.3390/m967}
}
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MLA
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Zissimou, Georgia A., and Panayiotis A. Koutentis. “N1-(5-Fluoro-2,4-dinitrophenyl)-N2-phenyl-4-(trifluoromethyl)benzene-1,2-diamine.” MolBank, vol. 2017, no. 4, Dec. 2017, p. M967. https://doi.org/10.3390/m967.