CuO and Ag2O/CuO catalyzed oxidation of aldehydes to the corresponding carboxylic acids by molecular oxygen

Article abstract of DOI:10.3390/molecules13040948

Furfural was oxidized to furoic acid by molecular oxygen under catalysis by 150 nm-sized Ag₂O/CuO (92%) or simply CuO (86.6%). When 30 nm-size catalyst was used, the main product was a furfural Diels-Alder adduct. Detailed reaction conditions and regeneration of catalysts were investigated. Under optimal conditions, a series of aromatic and aliphatic aldehydes were oxidized to the corresponding acids in good yields.

Full text of DOI:10.3390/molecules13040948

Molecules 2008, 13, 948-957
molecules
ISSN 1420-3049
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Full Paper
CuO and Ag O/CuO Catalyzed Oxidation of Aldehydes to the
2
Corresponding Carboxylic Acids by Molecular Oxygen
Qingyong Tian, Daxin Shi and Yaowu Sha *
The Key Laboratory of Bioorganic Phosphorous Chemistry and Chemical Biology, Department of
Chemistry, Tsinghua University, Beijing 100084, P.R. China
*
Author to whom correspondence should be addressed; E-mail: shayw@tsinghua.edu.cn
Received: 6 April 2008; in revised form: 17 April 2008 / Accepted: 17 April 2008 / Published: 21 April
008
2
Abstract: Furfural was oxidized to furoic acid by molecular oxygen under catalysis by 150
nm-sized Ag O/CuO (92%) or simply CuO (86.6%). When 30 nm-size catalyst was used,
2
the main product was a furfural Diels-Alder adduct. Detailed reaction conditions and
regeneration of catalysts were investigated. Under optimal conditions, a series of aromatic
and aliphatic aldehydes were oxidized to the corresponding acids in good yields.
2
Keywords: CuO, Ag O/CuO, catalyzed oxidation.
Introduction
The transformation of aldehydes to carboxylic acids is an important reaction in organic synthesis.
The commonly used oxidants for this transformation are NaClO [1-7], K Cr [8-9], pyridinium
chlorochromate [10], quinolinium dichromate [11-13], KMnO [14-16], H O [17-18] and so on.
2
2
2 7
O
4
2
2
3 2 2
Organic solvents such as CH CN, CH Cl , cyclohexane, formic acid and benzene are usually needed.
Although some of them have been widely used, they still have several disadvantages: low selectivity,
environmental contamination and so on. Catalytic oxidation by molecular oxygen is an eco-friendly
2 2 2
method. However, most reported catalysts such as Ru/CeO [19] and Ag O/Cu O [20] are too
expensive or difficult to prepare. Comparatively, Ag O/Cu O is an economical catalyst. Even so, it
2
2

Molecules 2008, 13
949
still needs to be regenerated, and there are no reports on its use for the above purpose, because it is
almost impossible to keep Cu O unchanged at high temperature.
2
Furoic acid, an important intermediate, is mainly obtained by oxidation of furfural. A series of
reagents have been developed for this reaction, such as chromium species [9, 11, 13, 21, 22] and
chlorite [2, 3, 23]. For the reasons mentioned above, we first investigated the oxidation of furfural to
2
furoic acid by oxygen catalyzed by Ag O/CuO. Detailed reaction conditions and catalyst regeneration
were studied. In order to demonstrate the applicability of this method, some other aromatic aldehydes
were oxidized to the corresponding aromatic carboxylic acids under optimized conditions in good
yields. We also found that 150 nm-size CuO could catalyze the oxidation in a comparative yield to that
obtained with an Ag O/CuO system. This method has been used in industrial production of furoic acid.
2
Results and Discussion
Reaction conditions: Reaction temperature
Sodium hydroxide is needed to transform the formed acid to its salt, which is soluble in water.
Otherwise the catalyst will be encapsulated by the formed acid. Aldehydes can undergo Cannizzaro
reaction under basic conditions. The temperature has different effects on the kinetics of the desired
oxidation and the undesired Cannizzaro reaction. Thus, it is crucial to find a suitable temperature for
the reaction. As shown in Figure 1, the best temperature for both CuO and Ag O/CuO catalyzed
2
oxidation of furfural to furoic acid was 70˚C, while higher temperatures would decrease the adsorption
of oxygen and give faster side reactions.
Figure 1. Effect of reaction temperature on furoic acid yield.
95
90
85
80
75
70
65
CuO
Ag O/CuO
2
50
55 60 65 70 75 80 85
o
Reaction temperature ( C)
pH value
Acid can react with the catalyst to form corresponding silver and copper carboxylates which can
inhibit the catalytic reaction. Therefore, it is essential to neutralize the formed acid. Meanwhile, as
mentioned above, alkali will promote the undesired Cannizzaro reaction of aldehydes. The effects of

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950
pH on the oxidation are shown in Figure 2. The optimal pH value was 13. The experiments were
carried out at 70˚C.
Figure 2. Effect of pH value on furoic acid yield.
95
90
85
80
75
70
65
CuO
Ag O/CuO
2
10
11
12
pH value
13
14
Amount of catalyst
More catalyst can shorten the reaction time and raise the yield. However, the reaction rate is also
controlled by other conditions, such as the distribution of oxygen. Figure 3 shows that when the
catalyst was increased to 30% wt of the mixture, the yield of furoic acid reached its maximum.
Figure 3. Effect of catalyst amount on furoic acid yield.
92
90
88
86
84
82
80
78
CuO
Ag O/CuO
2
15
20
25
30
35
Percentage of catalysts (%)

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951
Size of catalyst
In general, a smaller-sized catalyst will have a larger specific surface area and a better catalytic
activity [24]. However, this was not the case in the Ag O/CuO and CuO-catalyzed oxidation of
2
2
furfural to furoic acid. When small nano-scale CuO and Ag O/CuO (30 nm, Figure 4) powder were
used, the main product showed a molecular weight of 300 by ESI-MS (Figure 5). Its structure is shown
in Figure 6. This result suggests that small nano-scale CuO and Ag O/CuO catalyze the Diels-Alder
2
reaction more efficiently than the oxidation of aldehydes.
Figure 4. TEM spectra of different sizes of CuO.
Figure 5. Mass spectrum of the Diels-Alder reaction product.

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Figure 6. Product of the reaction catalyzed by 30 nm CuO and Ag O/CuO.
952
2
OH
O
OHC
CHO
O
O
O
Cation poisoning
Catalysts are always sensitive to certain cations. When deionized water was replaced with running
2
+
water, no furoic acid could be obtained. Detailed experiments showed that Ca inhibited the reaction
2
+
+
+
2+
3+
and Mg just made the product darker while Na , K , Cu and Fe did little harm.
Catalyst regeneration and aging
Catalyst regeneration is essential for industrial production. The recycled catalyst could not be used
directly because some organic matter was adsorbed on the catalyst and part of the CuO had been
reduced to Cu O and Cu (Figures 7 and 8). The recycled catalyst was first washed with hot deionized
2
water to get rid of most organic adsorbates. Calcination was then performed to oxidize the reduced
Cu
2
O and Cu to CuO.
2
Figure 7. XRD spectra of Ag O/CuO; a) newly prepared; b) used 8 times; c) used 18
#
o
times; peaks with * are from Cu
2
2
O, are from Cu, are from Ag O.
#
*
*
0
*
c
*
#
*
*
b
a
10
20 30 40 50 60 70
2
θ/o

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953
Figure 8. XRD spectra of CuO: d) newly prepared; e) used 3 times; peaks with * are
#
from Cu O, are from Cu.
2
*
*#
*
#
*
*
e
d
20
30 40 50 60 70 80
o
2θ/
Figure 9. Effect of CuO recycling temperature on furoic acid yield.
90
85
80
75
70
65
5
00oC
4
4
3
50oC
00oC
50oC
300oC
2
2
50oC
00oC
1
2
3
4
5
Recycle times
Experiments showed that the calcination temperature greatly affected the recovery of catalyst
activity and the optimal temperature was around 250 °C (Figure 9).
With recycling, the catalyst aged gradually. The product acid could erode the catalyst and cause
remodification of the catalyst surface. Calcination also caused a granular aggregate of CuO powder
(
Figure 10). These factors caused the specific surface area of CuO powder to decrease, so less oxygen
could be adsorbed. For the Ag O/CuO catalyst, friction also caused Ag O to desquamate from the CuO
2
2
(
Figure 10). Therefore, the catalysts gradually became aged, as shown in Figure 11.

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954
Figure 10. TEM spectra of the catalyst Ag O/CuO; a) used 3 times; b) used 18 times.
2
Figure 11. Effect of number of Ag O/CuO recycling times on furoic acid yield
2
95
90
85
80
75
70
65
60
0
2
4
6
8 10 12 14 16 18
Recycle Times
Application of the catalysts
Ag
2
O/CuO and CuO could also catalyze the oxidation of other aromatic aldehydes to their
O/CuO always gave better results. Comparatively, CuO has
corresponding acids in good yields. Ag
2

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955
many special advantages, such as low cost, easy preparation and regeneration. The results are shown in
Table 1.
Table 1. Oxidation of aromatic aldehydes to corresponding carboxylic acids
Aldehyde
Furfural
Catalyst
Ag O/CuO
CuO
Ag O/CuO
Yield of carboxylic acid/%
2
92.0
86.6
Furfural
Benzaldehyde
Benzaldehyde
2
74.5
CuO
66.0
4
4
4
4
4
4
-OH-3-MeO-benzaldehyde
-OH-3-MeO-benzaldehyde
-Nitro-benzaldehyde
Ag O/CuO
81.3*
76.0*
78.6**
71.5**
73.4
2
CuO
Ag O/CuO
2
-Nitro-benzaldehyde
CuO
-MeO-benzaldehyde
Ag
2
O/CuO
-MeO-benzaldehyde
CuO
64.2
*
*
Ethanol was added to dissolve 4-hydroxy-3-methoxybenzaldehyde.
*Toluene was added to dissolve 4-nitrobenzaldehyde.
Conclusions
2
Under optimized conditions, 150 nm-size Ag O/CuO and CuO can catalyze the oxidation of
aromatic aldehydes to their corresponding carboxylic acids by molecular oxygen in good yields.
Obviously, CuO is a better choice for the industrial production in that it can be easily collected and
regenerated. Small nano-scale (30 nm) CuO and Ag
instead of the oxidation of furfural.
2
O/CuO catalysts favor Diels-Alder reactions
Experimental
General
All chemical reagents were of analytical grade. XRD experiments were carried out on a D8
Advance Bruker X-ray Diffractometer with monochromatized CuKα (λ=1.5418 Ǻ) radiation. The
morphology and particle size were measured using a Hitachi H-800 transmission electron microscope
1
13
(
TEM). The accelerating voltage of the electron beam was 200 kV. H- and C NMR spectra were
recorded on a JEOL JNM ECA-300 (300 MHz) instrument. Mass spectra were obtained on a Bruker
ESQUIRE-LC.
2
Preparation of Ag O/CuO
3
CuO (150 nm) powder (23.7 g) was added to a solution of AgNO (1.83 g) in deionized water (20
mL). After stirring well for 10 minutes, the mixture was heated to vaporize the water. The precursor

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was then calcined at 400 ˚C for 3 hours to promote the decomposition of AgNO . The heating rate was
3
maintained at 5 ˚C/min.
Oxidation of aldehydes
To a 500 mL five-necked round bottom flask were added catalyst (5 g) and deionized water (150
mL). Solutions of NaOH (6 g) in deionized water (30 mL) and aldehyde (0.15 mol) were placed
separately in two constant pressure dropping funnels. Then oxygen was blown into the flask while ts
contents were heated and vigorously stirred. When the temperature reached 70 ˚C, the NaOH aq and
the aldehyde were dropped into the flask in proportional amounts. It took about 20 min to add all the
reagents while the temperature was kept at 70 ˚C. After that, the mixture was filtered to recycle the
catalyst. 30% (wt) H SO (25 mL) was added to the filtrate while stirring. The product precipitated and
2
4
was filtered, washed with water and dried. The used catalyst was first washed thoroughly with hot
water to remove adsorbates. Then the catalyst was calcined for regeneration.
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