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Straightforward one-pot synthesis of benzofuroxans from o-halonitrobenzenes in ionic liquids

Aleksei Borisovich Sheremetev 1
Aleksei Borisovich Sheremetev
, 
Natal'ya Stepanovna Aleksandrova 1
Natal'ya Stepanovna Aleksandrova
, 
Nikolai V Ignat'ev 2
Nikolai V Ignat'ev
, 
Michael Schulte 2
Michael Schulte
2 Ionic Liquid Research Laboratory, Merck KGaA, Darmstadt, Germany
10.1016/j.mencom.2012.03.015
Published 2012-02-27
Communication , Volume 22, Issue 2, 95-97
19
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Sheremetev A. B. et al. Straightforward one-pot synthesis of benzofuroxans from o-halonitrobenzenes in ionic liquids // Mendeleev Communications. 2012. Vol. 22. No. 2. pp. 95-97.
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Sheremetev A. B., Aleksandrova N. S., Ignat'ev N. V., Schulte M. Straightforward one-pot synthesis of benzofuroxans from o-halonitrobenzenes in ionic liquids // Mendeleev Communications. 2012. Vol. 22. No. 2. pp. 95-97.
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TY - JOUR
DO - 10.1016/j.mencom.2012.03.015
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.03.015
TI - Straightforward one-pot synthesis of benzofuroxans from o-halonitrobenzenes in ionic liquids
T2 - Mendeleev Communications
AU - Sheremetev, Aleksei Borisovich
AU - Aleksandrova, Natal'ya Stepanovna
AU - Ignat'ev, Nikolai V
AU - Schulte, Michael
PY - 2012
DA - 2012/02/27
PB - Mendeleev Communications
SP - 95-97
IS - 2
VL - 22
ER -
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@article{2012_Sheremetev,
author = {Aleksei Borisovich Sheremetev and Natal'ya Stepanovna Aleksandrova and Nikolai V Ignat'ev and Michael Schulte},
title = {Straightforward one-pot synthesis of benzofuroxans from o-halonitrobenzenes in ionic liquids},
journal = {Mendeleev Communications},
year = {2012},
volume = {22},
publisher = {Mendeleev Communications},
month = {Feb},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.03.015},
number = {2},
pages = {95--97},
doi = {10.1016/j.mencom.2012.03.015}
}
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Sheremetev, Aleksei Borisovich, et al. “Straightforward one-pot synthesis of benzofuroxans from o-halonitrobenzenes in ionic liquids.” Mendeleev Communications, vol. 22, no. 2, Feb. 2012, pp. 95-97. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2012.03.015.

Abstract

Treatment of o-halonitrobenzenes with sodium azide in a [empyrr][BF4]/Bu4NBr/H2O system gives benzofuroxans in high yields, with the recovery and reuse of the ionic liquid for at least ten times.

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