Cathodic hydrodimerization of nitroolefins

Summary Nitroalkenes are easily accessible in high variety by condensation of aldehydes with aliphatic nitroalkanes. They belong to the group of activated alkenes that can be hydrodimerized by cathodic reduction. There are many olefins with different electron withdrawing groups used for cathodic hydrodimerization, but not much is known about the behaviour of the nitro group. Synthetic applications of this group could profit from the easy access to nitroolefins in large variety, the C–C bond formation with the introduction of two nitro groups in a 1,4-distance and the conversions of the nitro group by reduction to oximes and amines, the conversion into aldehydes and ketones via the Nef reaction and base catalyzed condensations at the acidic CH bond. Eight 1-aryl-2-nitro-1-propenes have been electrolyzed in an undivided electrolysis cell to afford 2,5-dinitro-3,4-diaryl hexanes in high yield. The 4-methoxy-, 4-trifluoromethyl-, 2-chloro- and 2,6-difluorophenyl group and furthermore the 2-furyl and 2-pyrrolyl group have been applied. The reaction is chemoselective as only the double bond but not the nitro group undergoes reaction, is regioselective as a ß,ß-coupling with regard to the nitro group and forms preferentially two out of six possible diastereomers as major products.


Introduction
Olefins being activated by an electron withdrawing group can be hydrodimerized by cathodic reduction [1,2]. Thereby, the cathode serves as cheap, versatile, immobilized and mostly nonpolluting reagent providing economical and ecological advantages compared to chemical reducing agents [3,4]. Alkenes with a large variety of electron withdrawing groups have been explored in cathodic hydrodimerizations (Scheme 1) [1,2]. We were interested in the nitro group as a substituent. It can be easily introduced by addition of a nitroalkyl anion to a carbonyl group followed by elimination of water from the resulting alcohol. The nitroolefin can be reduced at the nitro group, at the double bond and simultaneously at both groups. In acidic medium the nitro group is reduced between −0.25 V to −0.55 V vs SCE to mixtures of syn/anti-oximes in 85% to 92% yield at a mercury pool cathode and with slightly lower yields at a graphite cathode [5][6][7][8]. The current controlled reduction of alkyl-and aryl-substituted nitroalkenes in acidic medium affords mixtures of ketones and oximes in yields of 39% to 72% [9] and 55% to 91% [10], respectively.
The hydrodimerization of nitro olefins should lead to 1,4-dinitroalkanes following the regioselectivity found in other hydrodimerizations of activated olefins [1,2]. Thereby, the proton concentration in the electrolyte should be not too high, as otherwise the reduction of the nitro group to oximes would be favoured. On the other side the electrolyte should not be aprotic as protons are required for protonation of the intermediate anions in the reductive dimerization (Scheme 1).
According to the proposed mechanism for the cathodic hydrodimerization the radical anion b formed by one electron reduction of the substrate a, has three pathways for dimerization [1,2]. In path (I) protonation followed by one-electron reduction leads to anion c, which in a Michael addition with substrate a forms the anion d, which is protonated to hydrodimer f. In path (II) b undergoes a nucleophilic addition to a forming a dimer radical anion that is reduced to e that is then protonated to the dimer f. In path (III) the radical coupling of two radical anions b leads to the dianion e, which is protonated to the product.
We first checked the cathodic reduction of (E)-2-nitro-1-phenyl-1-propene (1) [for chemical formulas see Table 4] whether the dimer 2,5-dinitro-3,4-diphenylhexane (2) can be obtained and which would be the optimal conditions for a high selectivity and yield. The optimization and subsequent hydrodimerization of eight nitro olefins has been previously reported in [6][7][8]. There have been reports on the reductive dimerization of nitro alkenes prior to 1991. 1,4-Dinitro-2,3-diphenylbutane (3) has been obtained in less than 20% yield in the catalytic hydrogenation of β-nitrostyrene (4) [11]. Hydrodimerization of 4 was observed in enzymatic reduction [12]. Furthermore 3 was found in the reduction of 4 with TiCl 3 [13,14]. High dimer yields are reported for the reduction of several nitro olefins with the dianion of cyclooctatetraene [15]. ß-Nitrostyrene (4) has been reductively dimerized with organomanganese reagents to 3 in low yield [16]. The electrochemical reduction of 1-nitroalkenes was studied by cyclic voltammetry and controlled potential coulometry. The reduction probably proceeds by initial formation of the radical anion, which subsequently dimerizes [17]. Later conditions were described to achieve selectively either a cathodic ß,ß-coupling (cathodic hydrodimerization) or a α,ßcoupling with aliphatic nitro alkenes having acidic α-protons. ß,ß-Coupling can be achieved in good to high yield (41-95%) at high current densities [18]. In the reduction of 3,3-dimethyl-1nitrobut-1-ene the intermediate radical anion has been identified by ESR. Nitroalkene 4 is reported to be converted quantitatively to the hydrodimer 3 with SmI 2 [19]. A catalytic reductive β,β-carbon coupling of nitroalkenes catalyzed by a N-heterocyclic carbene has been reported recently. Diastereomers are formed, whose dr (d,l-over meso-ratio) ranges between 66:34 to 90:10. The interesting new reaction proceeds through a radical anion of the nitroalkene generated in a catalytic redox process. For ß-isopropyl-nitroethylene the radical anion has been identified by ESR [20].

Results and Discussion
Investigation of the cathodic hydrodimerization of nitroalkene 1 to hydrodimer 2 The cathodic hydrodimerization is performed in a divided electrolysis cell by variation of the electrolyte (Table 1, Scheme 2). The working potential was chosen from cyclic voltammetry and current/voltage curves in the cell used for the preparative conversion. The potential in the controlled potential electrolysis was −0.9 V to −0.95 V vs SCE. The results indicate: an increased acidity favours the formation of oxime 5 (Table 1, Nr. 1), whilst without a proton donor the olefin presumably is polymerized to a large extent (Table 1, Nr. 2). The addition of acetic acid in portions appears to be a good choice as a too high proton concentration is avoided and the necessary amount of protons is continuously provided in the proper amount. TEA-pTos appears to be a better supporting electrolyte than TBABF 4 : In the latter hydrogen bonds between the fluorine atoms and water possibly increase the water concentration in the double layer and this way reverse partially the hydrophobic effect of the alkyl groups in the tetraethylammonium cation. The dimer yield should increase with increasing radical concentration, which means that at the beginning of the reaction the dimer yield should be higher than towards the end. As olefin 1 and dimer 2 are expected to have a higher oxidation potential than DMF due to the nitro group the advantageous use of an undivided cell appears to be possible. Taking the optimal conditions of electrolysis Nr. 5 in Table 1 the influence of the parameters mentioned above was investigated ( Table 2).
The influence of the temperature is less significant than expected. The increase of the temperature to 50 °C shows a marginal increase of the yield, whilst a temperature decrease is more successful. Best results could be achieved at 0 °C. The yield after 50% charge consumption based on conversion is insignificantly higher ( Table 2, Nr. 9). This indicates that there is no higher yield at higher substrate concentration in the first half of the reaction compared to the second half. However, a remarkable increase of the yield is obtained in an undivided cell without addition of a proton donor. With a quantitative conversion of 1 the dimer 2 is obtained in 88% material yield and 90% current yield. Presumably the protons are generated at the anode by oxidation of residual water and/or the solvent DMF. A major source of residual water could be the very hygroscopic tosylate as one of the reviewers suggested. The conditions of Nr. 11 in Table 2 should be suitable for the conversion of further nitroalkenes.  [23]. d Ref. [24]. e Crude yield higher, product decomposes slowly during recrystallization.
The cyclovoltammogram (CV) of 1 shows two irreversible reduction peaks at −1.08 V and −1.8 V vs SCE. The second peak can be attributed to the reduction of hydrodimer 2, as for isolated 2 the reduction peak is found at this potential. The first peak can be assigned to the reduction of 1 forming the radical anion. Addition of acetic acid shows no potential shift but a slight increase of the peak current. This could indicate that the radical anion is fast protonated and the resulting radical is further reduced. Proton addition, however, could also favour the reduction of the nitro group to the oxime, which consumes four electrons. Decreasing hydrodimer yields with increasing temperature could be due to the existence of chemical side reactions of the radical anion, such as oligomerization or protonation, which are more accelerated at higher temperatures compared to the radical dimerization. It should be mentioned that at the cathode deep red species are formed that become colorless upon addition of acetic acid. In an undivided cell and an unstirred electrolyte, which allows diffusion between the electrodes, a red colour appears at the cathode, which disappears at the anode. This indicates the formation of coloured nitroalkyl anions and their decolourization by protonation.
The nitroalkenes were obtained by condensation of aldehydes with nitroalkanes (Scheme 3, Table 3) [21,22]. For work-up unreacted aldehyde was removed by way of the bisulfite adduct, this facilitated the crystallization and improved the yields. The preparation of the nitroalkenes 1, 4, 8, 9 is described in [25]; the IR, 1 H NMR, and MS data are provided in the experimental part (Supporting Information File 1). From a comparison of the experimental δ value for the vinylic proton with this from an increment calculation the cis position of the hydrogen atom to the nitro group can be assigned for the nitroalkenes 1, 8, 9, which is the E-configuration.
As the trifluoromethyl compound 10 is not accessible by the method A or B it is prepared in two steps from aldehyde 6c via the n-butylazomethine [24]. Particularly difficult was the synthesis of 12, where a product mixture is formed; additionally 12 decomposes partly during purification by fractional crystallization, furthermore it is air sensitive. All that leads to low yields of 12. The dinitrodiene 16 was prepared from 1,4-dinitrobutane and two equivalents of benzaldehyde with 1,2-diaminoethane as catalyst in 59% yield [26]; 1,4-dinitrobutane was prepared from 1,4-dibromobutane [27]. The structures of the prepared compounds were secured by comparing the melting points with these from the literature [24][25][26][27] and their spectroscopic data. The nitroolefins 10-15 exhibit the same spectroscopic features as these of 1, 4, 8, 9. The C,H,N and C,H,F,N analyses additionally confirm the structures. From the 1 H NMR spectra for all nitro olefins the E-configuration of the double bond can be derived.

Cyclic voltammetry
The reduction potentials (E p,c ) of the nitroalkenes were determined by cyclic voltammetry. The values, ordered by decreasing potentials, are shown in Scheme 4.
The reduction potentials E p,c are determined by the conformation of the aryl group, the electron density at the double  [28]. The more positive potential of 16 compared to 1 could be due to intramolecular interactions of the nitro groups with the non-conjugated double bonds. The E p,c of 1 and 4 measured at an amalgamated gold-wire electrode in DMF are somewhat more positive than those measured at a Pt-disc in ACN [17].
In the CV of all nitroolefins a second reduction peak appears at a potential being 600-800 mV more cathodic compared to the first one. Possibly this is the reduction of the hydrodimer as the CV of the hydrodimer of nitroolefin 1 indicates. This is different for the nitroolefins 14 and 15, which are o,o'-disubstituted at the phenyl ring ( Figure 1).
In the CV of 14 and 15 (Figure 1a) already at low scan rates (0.1 V/s) an anodic peak (E p,a = −0.95 V for 14 and E p,a = −0.92 V for 15) appears in the reverse scan. Reversing the scan after the first peak leads for 15 at a scan rate of 10 V/s to a CV peak with E p,c = −1.084 V, E p,a = −0.904 V and i p,c /i p,a = 1. For 14 higher scan rates were necessary to achieve a similar effect, but there the curve became strongly distorted possibly due an increasing capacitive current and iR-drop. This indicates, that most probably due to the o,o-substituents in 15 the follow-up reaction of the radical anion is slowed down for steric reasons. For 14 no dimer was found (see below). Further electroanalytic investigations were omitted in favour of the preparative scale hydrodimerizations of the nitroolefins.

Preparative scale electrolyses at the Hg cathode
The preparative scale electrolyses were performed using the following conditions: Hg cathode, undivided cell, 0.2 M TEA-pTos in DMF at 0 °C, cathode potential of −0.90 V to −0.95 V vs SCE. These conditions were optimal for the potential controlled conversion of nitroolefin 1 into dimer 2. The conversions shown in Table 4 consumed one charge equivalent    The smaller space filling of the fluorine atom compared to the chlorine atom should lead to a sterically less hindered radical anion in the reduction of 15, which allows the formation of 40% of the dimer 29 and leads to less oxime and nitro alcohol as side products (Scheme 5b).
The dimers 2 and 18-23 could be identified by 1 H, 13 C NMR, MS and elemental analyses (see Structures of the hydrodimers and Experimental part in Supporting Information File 1). Dimer 3 is insoluble in common solvents at rt, thus no 1 H and 13 C NMR could be obtained. It has a correct elemental analysis and the IR spectrum is similar to this of 2 and the other dimers with regard to the NO 2 group. It melts at 238-242 °C with decomposition, which is similar to the product obtained by hydrogenating dimerization of olefin 4 in [11]. The insolubility and the melting point disagree, however, with compound 3 (n = 1) described in [20]. From the laser desorption ionization (LDI) mass spectrum of 3 it could be presumed that 3 is mainly a trimer (3, n = 2). The trimer could arise by a Michael addition of the intermediate dimer radical anion or dimer dianion of 4 to olefin 4. Indications to greater portions of 3 (n = 1) and 3 (n = 3) were not found in the LDI-MS. Support for this assumption comes from coulometry for 4 in [17], which indicates oligomerization. Oligomerization does not occur if the substituent α to the nitro group is an alkyl group as in olefin 1, possibly due to steric hindrance.
The dinitrodiene 16 is intramolecularly coupled at the Hg cathode to form the dinitrocyclohexane 30 (Scheme 6a), it also does not show the usual behaviour found in the preceding elec- trolyses. A significant decrease of the current is only found after a current consumption of 2.96 F/mol. Except for benzaldehyde no further side products were detected. 30 is formed as mixture of diastereomers, which could not be separated by flash chromatography. The aliphatic nitroalkene 17 could be hydrodimerized in 68% yield to the hydrodimer 31, which is a mixture of diastereomers. Partial separation by flash chromatography and 1 H NMR spectroscopy of the fractions indicates four diastereomers in a ratio of about 38:9:14:1.
It is possible to substitute the cathode material mercury against the environmentally benign graphite. At a graphite cathode the nitroolefin 1 could be hydrodimerized to the dimer 2. With 60% the yield is lower than in the reduction at the Hg cathode, where 88% of the dimer were obtained. Possibly higher yields can be obtained with other graphite varieties or other nontoxic cathode materials. But in principle the mercury cathode can be replaced by a graphite cathode.

Structure of the hydrodimers
All products show for the nitro group characteristic asymmetrical and symmetrical vibrations at 1530-1560 cm −1 and 1350-1360 cm −1 , which, compared to the educts, are shifted to shorter wavelengths.
The hydrodimers show in the upper masses of the mass spectra few fragments and these have a low intensity. The base peak in all hydrodimers results from breaking of the dibenzyl bond and loss of NO 2 affording the mass = (M + /2 − 46).
The C-C bond formation can lead to α,α-, α,β-and ß,ß-coupled products. The 1 H NMR spectra and MS data support in all cases a ß,ß-coupling. A α,β-or a α,α-coupling would lead to the occurrence of methyl singlets or non-coupled benzylic protons. Such signals were not observed in the spectra of the hydrodimers.
The stereochemistry of the hydrodimer results from a β,ß-C-C bond formation and from a α,δ-diprotonation, which creates a dimer with four stereocenters with the exception of dimer 3, which has only two stereocenters. This means 2 3 diastereomers can be formed, which are decreased to six diastereomers due to the identity of two pairs of enantiomers as shown in Scheme 7. Configurations could not be assigned, as data for comparison are not available in the literature and crystals for X-ray diffraction could not be obtained.
The dimers are obtained as mixtures of diastereomers; as they do not differ significantly in their MS and IR spectra the compounds had to be characterized by their 1 H NMR data. For that purpose the diastereomers were purified as good as possible by flash chromatography and/or HPLC. Single diastereomers are denoted alphanumerically (e. g., 2a, 2b). The same letter means for two diastereomers of different hydrodimers that they have similar NMR spectra with regard to chemical shift and multiplicity. This corresponds to a similar rate of elution in chromatography.

H NMR spectra
For the hydrodimers 2 and 18-23 five different diastereomers a-e can be identified. In Table 5 the 1 H NMR data of the five diastereomers 2a-e are assembled.
The diastereomers show remarkable differences in the chemical shifts. This also holds for significant differences in the chemical shifts for formally identical protons in 2b/e. The considerable differences probably result from the anisotropy effect of the aromatic ring and the nitro group. For the nitro group a similar anisotropic cone as for the carbonyl group is assumed [30]. Due to the presence of two nitro and two phenyl groups conformations are possible, where protons are in shielded and unshielded areas. Also phenyl protons appear as broad, high field shifted signals. For 18c a ratio of high field and normal signals of 4:6 was found. With decoupling experiments they can be clearly assigned to be phenyl protons. Comparable results, as shown for 2, were found for the mixtures of diastereomers of the other hydrodimers. Besides decoupling experiments also 1 H NMR simulations give valuable support to assign the complex coupling pattern. This is shown for 18b where the complexity of the spectrum is strongly increased by the diastereotopic methylene protons (Figure 2).
The ratios of diastereomers for the products 2 and 18-23 are summarized in Table 6.
The main part of the mixture consists usually of the isomers a and b. Dimer 22 is an exception being possibly caused by the NH groups of the pyrroles. Their hydrogen bonds could influence the relative energies of the transition states leading to the diastereomers. One of the two meso-configurations can be assigned to isomer 22a because of the missing coupling between the benzylic methine protons.   The 1 H NMR data obtained for 29-31 are compatible with the shown structures.

C NMR spectra
The proposed structures were confirmed by their 13 C NMR spectra. Nearly all diastereomers can be characterized via their 13 C signals. The regioselective ß,ß-linkage follows clearly from the multiplicities of the carbon atom resonances. Signals of aliphatic quaternary carbon atoms were not detected. The differences between the signals of single diastereomers of a dimer correlate very well with the results of the proton resonance experiments. The measured values agree quite well with increment calculations (Table 7) [31].

Elemental analyses
The structures could be secured additionally by elemental analyses and in the case of dimer 20 by high resolution MS. They were obtained from the mixtures of isomers taking into account all elements (C, H, N, halogen).

Conclusion
The potential controlled cathodic hydrodimerization of 1-nitroalkenes affords a one step electrochemical C-C bond formation to 1,4-dinitro compounds. Applying optimized conditions the hydrodimers are obtained in good to very good yields. Besides mercury also graphite can be used as cathode material. The scope of the reaction is demonstrated in ten nitroalkenes with different 1-aryl and mostly 2-methyl substituents. Likewise the cathodic cyclization of a dinitrodiene could be realized.
The dimerization is chemoselective: the fairly easy reduction of the nitro group can be suppressed and aryl C-Cl and aryl C-F bonds are not cleaved. Additionally a good regioselectivity is obtained, among the possible three coupling products only the ß,ß-linked dimer is found. The diastereoselectivity is moderate, one obtains two main diastereomers (about 70-80% of the mixture of isomers) and one of the six possible diastereomers was not found.
The use of an undivided cell facilitates the electrolysis and lowers the energy consumption. For the preparation of dimer 2 in an undivided cell at cell voltages of 10-15 V, one needs 1.8-2.7 kWh/kg of product, which is much below the 8 kWh/kg, where a technical electrolysis becomes favourable with regard to the energy consumption [32,33].

Supporting Information
Supporting Information File 1 Experimental procedures, 1 H, 13 C NMR and MS spectra and elemental analyses.