TETRAHEDRON

LETTERS
Pergamon Tetrahedron Letters 42 (2001) 6767–6769

A fast and mild method for the nitration of aromatic rings

Radoslaw R. Bak and Andrew J. Smallridge*
School of Life Sciences and Technology, Victoria University of Technology, PO Box 14428, Melbourne 8001, Australia
Received 20 June 2001; revised 18 July 2001; accepted 26 July 2001

Abstract—The use of N2O5 and a Fe(III) catalyst for the nitration of aromatic rings is described. This methodology is compatible
with most functional groups and results in near quantitative yields in 4 min. The reaction conditions are non-oxidising:
benzaldehyde and benzyl alcohols are readily nitrated with little or no oxidation (<4%) occurring. The addition of the iron catalyst
activates the system to such an extent that nitration of an activated aromatic ring, such as toluene, occurs quantitatively at
−100°C. This high activity allows compounds with sensitive functional groups such as alkenes to be smoothly nitrated. © 2001
Published by Elsevier Science Ltd.

Conventional methods for the nitration of aromatic quantitative yield of o- and p-nitrotoluene after only
rings utilize nitric acid or mixtures of nitric and sul- 10 min. Attempts to nitrate less activated aromatic
phuric acids. These conditions are incompatible with a rings, such as acetophenone, using this methodology
range of compounds which are sensitive to oxidising resulted in recovery of unreacted starting material.
or strongly acidic conditions. Use of nitronium salts,
such as those formed from methane sulfonic acid,1 or The use of an Fe(III) catalyst for the nitration of
from Lewis acids, such as boron trifluoride,2 are also aromatic rings using NO2 in the presence of oxygen has
hampered by liberation of strong acids; in the case of been reported.6 The iron activates the NO2 although
the boron trifluoride/nitronium salt, HF and BF3 are long reaction times, up to 72 h, are required and
liberated.2 moderately deactivated substrates are not nitrated. It
was thought that Fe(III) might also be capable of
For our studies a mild nitrating agent was required, catalysing nitration reactions using the more active
which could nitrate moderately deactivated aromatic N2O5.
rings in the presence of a variety of functional groups.
Recent developments in aromatic nitration methodol-
ogy using NO2/O3 (Kyodai nitration) demonstrated Table 1. Nitration of aromatic rings using N2O5 and
excellent conversions for a variety of aromatic com- Fe(acac)3 for 4 min
pounds.3 In the Kyodai nitration the active nitrating
agent is thought to be N2O5 which is formed in situ R R
N2O5
from NO2 and O3. The drawbacks to this method
include the necessity to generate ozone, which Fe(acac)3
NO2
limits the reaction rate, and long induction periods,
during which sensitive compounds may undergo degra-
R o:m:p Isolated yield (%)
dation.
CHO 18:60:22 93
The direct use of N2O5 as a nitrating reagent, instead COCH3 50:44:6 98
of generating it in situ, has been previously reported CH2CN 21:B1:79 96
for activated aromatic rings.4 In our hands N2O55 CH2OH 33:B1:67 91
readily nitrated toluene at 0°C to give a virtually Br 19:32:49 99a
NO2 B1:99:B1 94b
CN 68:32:B1 95b

a
Reaction conducted at 20°C.
b
* Corresponding author. Reaction conducted at 40°C.

0040-4039/01/$ - see front matter © 2001 Published by Elsevier Science Ltd.

PII: S 0 0 4 0 - 4 0 3 9 ( 0 1 ) 0 1 3 7 8 - 8
6768 R. R. Bak, A. J. Smallridge / Tetrahedron Letters 42 (2001) 6767–6769

Nitration of acetophenone at 0°C using Fe(acac)3 and of 2,4- and 2,6-dinitrotoluene. The mono-nitrated
N2O5 in dichloromethane resulted in a near quantita- product can be obtained by conducting the nitration
tive yield of o- and m-nitroacetophenone after only 4 reaction at −100°C (dry ice/ether bath) (Scheme 1). In
min.7 the absence of the iron the reaction occurs at 0°C,
this dramatic difference in reaction temperature
This nitrating procedure was found to be applicable clearly illustrates the activating effect of the iron cata-
to a range of aromatic compounds (Table 1). lyst.

In all cases complete nitration was observed after The ability to conduct the nitration reaction at such
only 4 min and the products were readily isolated in low temperatures allows the nitration of compounds
near quantitative yields.8 For some deactivated aro- containing functional groups which are themselves
matic rings (R=Br, NO2, CN) incomplete nitration susceptible to nitration. Nitration of ethyl cinnamate
was observed at 0°C. Conducting these reactions at at 0°C resulted in attack at the double bond leading
slightly elevated temperatures (20–40°C) resulted in to a complex mixture of products. However, conduct-
quantitative yields of nitrated product. These reaction ing the nitration reaction at −100°C (dry ice/ether
conditions are extremely mild as exemplified by the bath) for 4 min gave a quantitative yield of nitrated
ready formation of nitrobenzaldehyde, from benzalde- product, indicating the high reactivity of this method-
hyde, with no evidence of oxidation of the aldehyde ology (Scheme 2).
functionality. In the case of benzyl alcohol a small
amount of benzaldehyde (<4%) is formed. The structure of the active nitrating complex is not
clear nor is the mechanism of the reaction. Unlike
The regioselectivity of the nitration reaction is similar other nitrating systems involving Lewis acids,9 such as
to that observed for reactions conducted under stan- BF3, this reaction is clearly catalytic. Addition of
dard nitrating conditions, HNO3/H2SO4, except for N2O5 to a solution of Fe(acac)3 results in the forma-
nitration of compounds containing a carbonyl group, tion of a pale pink solid. Attempts to isolate and
e.g. benzaldehyde and acetophenone, which produce characterise this complex have to date been unsuc-
increased amounts of the o-isomer. Reactions con- cessful as the complex decomposes readily in moist
ducted under non-acidic conditions using N2O5 have air although it can be filtered and washed with
also been reported to exhibit this enhanced o-nitra- dichloromethane under nitrogen. This washed com-
tion.3 It has been postulated that in the absence of plex does not nitrate aromatic rings stoichiometrically
acidic protons the carbonyl group is not protonated in the absence of N2O5 but the reaction proceeds nor-
leading to o-nitration whilst the protonated carbonyl mally upon the addition of further amounts of N2O5.
group is meta directing. It is also critical to add the N2O5 to the Fe(III) to
form the complex prior to the addition of the aro-
Whilst deactivated aromatic rings are readily mono- matic substrate. If the complex is not preformed the
nitrated under these conditions, nitration of toluene, a nitration reaction is significantly slower, and similar
mildly activated aromatic ring, leads to the formation results are obtained to those in reactions conducted in
the absence of the Fe(III). Addition of substrate to
the nitrating complex causes an immediate colour
change to an intense red/brown colour, and the com-
NO2
plex dissolves. The nitration reaction is self-indicating
CH3 CH3 CH3
N2O5 as the mixture reverts to a lighter colour and the
+
Fe(acac)3
solid catalyst is reformed once nitration is complete.
-100°C
NO2 The use of N2O5 and Fe(acac)3 is a simple, fast and
mild procedure for the nitration of aromatic rings.
65 : 35 The reaction is tolerant of a range of functional
groups and gives virtually quantitative yields in less
Scheme 1. than 4 min.

NO2
CO2Et CO2Et CO2Et
N2O5
+
Fe(acac)3
-100°C
NO2
37 : 63

Scheme 2.
 R. R. Bak, A. J. Smallridge / Tetrahedron Letters 42 (2001) 6767–6769 6769

References liberates toxic nitrogen oxides. Small amounts can be

quickly neutralised with copious amounts of water.
1. Coon, C. L.; Blucher, W. G.; Hill, M. E. J. Org. Chem. 6. Suzuki, H.; Yonezawa, S.; Nonoyama, N.; Mori, T. J.
1973, 38, 4243. Chem. Soc., Perkin Trans. 1 1996, 2385.
2. Olah, G. A.; Malhotra, R.; Narang, S. C. Nitration Meth- 7. Addition of N2O5 (15 mmol) to a stirred solution of 10 ml
ods and Mechanisms; VCH: Cambridge, 1989; pp. 50–94. CH2Cl2 and Fe(acac)3 (0.1 mmol) at 0°C results in the
3. Suzuki, H.; Murashima, T. J. Chem. Soc., Perkin Trans. 1 formation of the nitrating complex as a light pink solid.
1994, 903. Substrate (5 mmol) is added to the reaction, which is
4. Furukawa, K.; Yoshizawa, F.; Akutsu, Y.; Arai, M.; stirred for 4 min at 0°C, and then quenched with 2 M HCl
Tamura, M. Kayaku Gakkaishi 1999, 60, 143. (20 ml) (water or Na2CO3 solution can also be utilized for
5. Freshly distilled fuming nitric (100%) was added slowly to acid sensitive substrates). The reaction was extracted with
a distillation flask containing P4O10. Slow distillation CH2Cl2 and washed with aqueous Na2CO3 and brine.
affords N2O5 with liberation of nitrogen oxides. The col- Removal of solvent afforded the pure nitrated compounds
lected N2O5 is placed in a freezer until a solid is formed, in near quantitative yields.
the product is then warmed slowly to 10°C at which time 8. All compounds were fully characterized using 1H and 13C
any liquid nitrogen oxides are discarded, to leave a white/ NMR.
yellow solid. It is important that the N2O5 used is free of 9. Bachman, G. B.; Dever, J. L. J. Am. Chem. Soc. 1958, 80,
nitrogen oxide(s) CAUTION: N2O5 is highly corrosive and 5871.