Reactivity of Aryl Halides for Reductive Dehalogenation in (Sea)water Using Polymer-Supported Terpyridine Palladium Catalyst

A polymer-supported terpyridine palladium complex was prepared. The complex was found to promote hydrodechlorination of aryl chlorides with potassium formate in seawater. Generally, reductive cleavage of aryl chlorides using transition metal catalysts is more difficult than that of aryl bromides and iodides (reactivity: I > Br > Cl); however, the results obtained did not follow the general trend. Therefore, we investigated the reaction inhibition agents and found a method to remove these inhibitors. The polymeric catalysts showed high catalytic activity and high reusability for transfer reduction in seawater.


Introduction
Following the adoption of the "Stockholm Convention on Persistent Organic Pollutants" in 2001 many countries prohibited the production and use of chloroarenes, including poly(chlorobiphenyls) (PCB), 3-(3,4-dichlorophenyl)-1,1-dimethylurea and dioxins [1,2]. However, environmental pollution caused by past use of chloroarenes persists. For example, in 2000, Haynes et al. reported that 3-(3,4dichlorophenyl)-1,1-dimethylurea [3], which was widely used in sugarcane (Saccharum) plantations, has caused atrophy of coral and seaweed beds in the Australian Great Barrier Reef [4][5][6]. The OPEN ACCESS chloroarenes released into the environment are present at levels of only parts per million in soils and seawater, and the collection and decomposition of chloroarenes is difficult. Therefore, we have attempted to develop a decomposition reaction for chloroarenes in seawater and establish a method to collect the low concentrations of chloroarenes released in seawater [7]. Hydrodechlorination of aryl chlorides has received considerable attention in chemistry, particularly from an environmental perspective. A large amount of research has been devoted to the synthetic application of the reaction as well as to improving its efficiency in homogeneous and heterogeneous conditions [1,2]. In addition, considerable research into the Pd-catalysed dehalogenation reaction in organic solvent and aqueous media [8][9][10][11][12][13][14][15][16][17][18][19][20] has been undertaken since Helquist first reported the reduction of aryl bromides by sodium formate catalysed by Pd(PPh3)4 in 1978 [21].
Our first study into hydrodechlorination of various aryl chlorides in seawater were conducted in the presence of an amphiphilic polystyrene-poly(ethylene glycol) (PS-PEG) resin-bound terpyridine-palladium catalyst and unexpectedly gave dechlorinated products in lower yield than yields in pure water (Table 1) [7]. In these studies, we were surprised to find that the reactive order of halides for the hydrodehalogenation of aryl halides in pure water was Ar-Cl > Ar-Br > Ar-I. For example, the hydrodehalogenation of p-bromoacetophenone and p-iodoacetophenone for 24 h gave dehalogenated products in 74% and 0.5% yield (Table 3, runs 2-3), although a dechlorinated product was obtained in quantitative yield in the case of p-chloroacetophenone [22]. In general, the reductive cleavage of aryl chlorides is more difficult than that of aryl bromides and iodides (reactivity: I > Br > Cl); however, the results obtained did not follow the general trend [8,10,13,[23][24][25][26]. Here, we report the anionic influence on the reactivity of hydrodehalogenation in pure water by using a polymer-supported Pd catalyst (Scheme 1).

Scheme 1.
Polystyrene-poly(ethylene glycol)-supported terpyridine-Pd complex and application to the hydrodehalogenation of aryl halides in the presence of anion inhibitors in water.

Results and Discussion
We developed the hydrodehalogenation of aryl chlorides, bromides and iodides in water using the polymeric catalyst 1, which was readily prepared from methyl 4-formylbenzoate, 2-acetylpyridine, NH4OH, PS-PEG-NH2 resin and (C6H5CN)2PdCl2 according to previously reported procedures [27]. The hydrodechlorination of p-chloroacetophenone (2a) was performed in pure water with HCO2K and polymeric catalyst 1 ( Representative results that allow a comparison between the results for seawater and those for water are summarised in Table 1. The reduction of 2a-c with HCO2K and polymeric catalyst 1 (5 mol % Pd) in seawater provided acetophenone (3a) in 44%-65% yield, whereas, when performed in water, a similar reaction gave 94%-96% yields ( Table 1, runs 1-3). The reduction of chlorobenzophenones 2d-f in seawater provided benzophenone (3b) in 52%-84% yield ( Table 1, runs 4-6, respectively). Reduction of chlorobenzene derivatives 2g-l, which have electron-donating substituents in the ortho-, meta-and para-positions, provided aniline 3c or phenol 3d in yields of 9%-90% (Table 1, runs 7-12). Dechlorination of highly chlorinated compounds 2m and 2n in seawater gave the corresponding product 3a in 58% and 90% yield, respectively ( Table 1, runs [13][14]. It was surprising to find that the reaction efficiency was noticeably affected by whether water or seawater was used. In general, various inorganic salts dissolve in seawater in contrast to pure water. Therefore, we examined halides that dissolve in seawater as catalytic inactivating agents to determine the reactivity of hydrodechlorination in water using a polymer-supported palladium catalyst. The results are summarised in Table 2. The hydrodechlorination of p-chloroacetophenone (2a) was performed in NaBr solution and NaI solution with HCO2K and polymeric catalyst 1 (5 mol % Pd) at 25 °C for 3 h to provide acetophenone (3a) in 63% and 66% yields ( Table 2, runs 4-5), whereas a similar reaction provided 94%-95% yield in water, NaF solution and NaCl solution (  The reaction proceeded smoothly when a silver bromide ion was precipitated in a silver nitrate solution ( Table 2, run 10). These results suggested that Br − and I − were reaction inhibiting agents for the hydrodechlorination of aryl halides in water. Due to the generated Br − or I − , the hydrodehalogenation of p-bromoacetophenone (2o) and p-iodoacetophenone (2p) did not proceed smoothly, and the desired product was obtained in 74% and 0.5% yield (Table 3, runs 2-3). However, unexpectedly, a quantitative yield of the dechlorinated product was obtained in the case of p-chloroacetophenone (Table 3, run 1). We proceeded to examine the reduction of aryl chlorides by increasing the reaction time under similar conditions. Thus, the reduction of 2a with HCO2K was performed with polymeric precatalyst 1 (5 mol % Pd) in seawater for 12 h to provide acetophenone (3a) in 94% yield (Table 2, run 12). All reactions were also carried out in seawater for 12 h to give dechlorinated products in 68%-95% yield (Table 1). Table 3. Hydrodehalogenation of acetophenone-4-halide with ammonium formate in water.  The recyclability of PS-PEG terpyridine Pd (II) 1 was examined for the hydrodechlorination of p-chloroacetophenone (2a) in seawater. After the first reaction, which provided acetophenone (3a) in 94% yield, the precatalyst was recovered by simple filtration, washed with H2O, dried under vacuum, and reused five times under similar reaction conditions to provide 3a in 95%, 96%, 95%, 95% and 96% yields, respectively. Inductively coupled plasma atomic emission spectroscopy analysis of the aqueous phase revealed barely detectable levels of palladium residue (<1 ppm).
To investigate the reduction of meta-chlorobiphenyl (2q) as a representative PCB using polymeric precatalyst 1, we also tested the reaction with HCO2K with polymeric precatalyst 1 in water at 100 °C for 24 h. This reaction provided biphenyl (3e) in 91% yield. This result demonstrates the efficient detoxification reaction of PCB in seawater, which is an environmental endocrine disrupter (Scheme 2).

General Methods
All manipulations were carried out under aerobic conditions. Water was deionised using a MilliQ gradient A10 apparatus (Millipore, Bedford, MA, USA) to Milli-Q grade. 1 H-and 13 C-NMR spectra were recorded in dimethyl sulfoxide-d6 (DMSO-d6) at 25 °C on an Avance spectrometer (400 MHz for 1 H and 100 MHz for 13 C, Bruker, Karsruhe, Germany). 13 C-NMR chemical shifts were given relative to the residual DMSO-d6 peaks used as an internal standard (77.0 ppm and 39.7 ppm, respectively). Mass spectral data were measured on a JMS-T100GCV mass spectrometer (MS) detector and a JMS-T100LP MS detector (JEOL, Tokyo, Japan); the abbreviation "bp" is used to denote the base peak. Gas chromatography (GC) analysis was performed on a GC-2014 GC (Shimadzu, Kyoto, Japan). Infrared spectroscopy (IR) analysis was performed on a FTIR-410 spectrometer (JASCO, Tokyo, Japan).

Synthesis of Polymer-Supported Ligand
A solution of aqueous NH4OH (28%, 0.2 mL) and NaOH (80 mg, 2.0 mmol) in minimum water was added to a solution of 4-methoxycarbonylbenzaldehyde (164 mg, 1.0 mmol) and 2-acetylpyridine (242 mg, 2.0 mmol) in EtOH (4.1 mL). After adding NaOH, the solution turned red after 1 h. The solution was stirred vigorously at room temperature in a flask exposed to air for 17 h, after which a

Conclusions
A new polymer-supported terpyridine palladium complex 1 has been developed through the formation of a covalent bound between the resin and the amino group. The resulting resin efficiently catalysed the hydrodechlorination of aryl chlorides with HCO2K in seawater under mild conditions to provide the corresponding products in up to 95% yield. We also describe the catalysis inactivation agents and a method to remove these inactivating agents, which were dissolved in seawater for the presented reaction. This is the first example of the hydrodechlorination of aryl chlorides in seawater in which a polymeric precatalyst has been employed. We are continuing to investigate the scope of the hydrodechlorination and possible applications of the precatalyst in other organic transformations.