Percia B. Arockiam, Cédric Fischmeister, Christian Bruneau* and Pierre H. Dixneuf*
Centre of Catalysis and Green Chemistry, OMC-Institut Sciences Chimiques de Rennes, UMR 6226: CNRS-Université de Rennes, Campus de Beaulieu, 35042 Rennes, France. E-mail: christian.bruneau@univ-rennes1.fr; pierre.dixneuf@univ-rennes1.fr
First published on 1st October 2012
The ruthenium(II)-phosphine catalyst RuCl2(PPh3)(p-cymene) operating water selectively leads to ortho monoarylation, with arylchlorides and heteroarylhalides, of functional arenes. Further catalytic heteroarylation with Ru(OAc)2(p-cymene) in water produces mixed bifunctional derivatives.
Selective monoarylations are easily achieved only when one ortho substituent is present or when only one C–H bond is protected by steric hindrance of a substituent at an arene meta position. However a few ruthenium(II)-phosphine catalysts operating in organic solvents have shown the ability to preferentially generate monoarylated arenes with rather good selectivity.4 The first example of direct arylation with arylbromides using the ruthenium(II)-PPh3 catalyst was shown by Oi and Inoue and led predominantly to the ortho monoarylation of 2-phenylpyridine and arylimines in NMP.4a,b Chanjuan Xi et al.4c demonstrated a selective monoarylation of 2-phenylpyridine in the presence of a [RuCl2(PPh2(–C(Ph)CHPh)(arene))] catalyst precursor. The [RuCl2(L)(p-cymene)]2 complex containing a bulky monophosphine L ligand was efficient to monoarylate 2-phenylpyridine and N-phenylpyrazole with arylchlorides in NMP at 120 °C as reported by Doherty et al.4d In parallel the carboxylate-ruthenium(II) catalysts when operating in water were revealed to provide in a rare example a high ratio of mono(hetero)arylation of functional arene C–H bonds.3c Thus we have investigated the positive influence of these two factors: ruthenium(II)-phosphine catalyst and ruthenium catalysis in water in the search for selective monoarylation, thus in a non-toxic solvent and under greener chemistry conditions. Several industrial processes are already operating under aqueous phase organometallic-catalyzed reaction conditions and there are already some technical solutions such as membrane filtration or phase separation for water recovery.5
We now report that Ru(II)-PPh3 catalyst RuCl2(PPh3)(p-cymene) operating in water, without a carboxylate promoter, constitutes a good catalytic system for selective monoarylation of functional arenes and that the sequential catalytic functionalisations in water of two ortho C–H bonds of functional arenes can be applied to reach unsymmetrical ortho diarylated arenes and one example of mixed ortho arylated and alkenylated arenes.
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Entry | Catalyst | Time (h)/Convb (%) | 3a/4ac |
---|---|---|---|
a Reaction conditions: 0.6 mmol of 2-phenylpyridine, 5 mol% of [Ru], 3 equiv. of K2CO3, 10 μL of tetradecane (internal standard) for GC, 0.5 mmol of chlorobenzene in 2 mL of water, 24 h, 100 °C.b Conversion determined by gas chromatography based on arylhalide.c 3a/4a ratio determined by gas chromatography.d Reaction at 80 °C.e Reaction performed in NMP as a solvent.f Reaction at 60 °C. | |||
1 | [RuCl2(p-cymene)]2 | 24 h – 97 | 78/22 |
2 | Ru(OPiv)2(p-cymene) | 24 h – 98 | 78/22 |
3 | Ru(OPiv)2(p-cymene) + 2 equiv. PPh3 | 24 h – 100 | 82/12 |
4 | Ru(OAc)2(p-cymene) | 24 h – 97 | 80/20 |
5 | Ru(OAc)2(p-cymene) + 2 equiv. PPh3 | 24 h – 89 | 94/6 |
6 | RuCl2(PPh3)(p-cymene) | 24 h – 100 | 89/11 |
7 | RuCl2(P(CH2Ph)3)(p-cymene) | 24 h – 98 | 85/15 |
8 | RuCl2(PCy3)(p-cymene) | 24 h – 94 | 89/11 |
9 | RuCl2(Pi-Pr3)(p-cymene) | 24 h – 93 | 85/15 |
10 | [RuCl2(p-cymene)]2 + (P(o-Me-C6H4)3) | 24 h – 96 | 80/20 |
11d | RuCl2(PPh3)(p-cymene) | 3 h – 81 | 96/4 |
5 h – 92 | 95/5 | ||
5 h – 45e | 98/2 | ||
12f | RuCl2(PPh3)(p-cymene) | 16 h – 70 | 98/2 |
The reactions produced only 3a and 4a derivatives without side products such as homocoupling products. With [RuCl2(p-cymene)]2 as the catalyst precursor in the absence of a carboxylate ligand a conversion of 97% was reached in 24 h with a 3a/4a ratio of 78/22 (Table 1, entry 1). The reaction performed in the presence of Ru(OPiv)2(p-cymene) and Ru(OAc)2(p-cymene), which were previously shown to be efficient catalysts for diarylation in water,3c,7 led to 97% conversion, with a moderate 3a/4a ratio (Table 1, entries 2, 4). Addition of 2 equiv. of PPh3 to the ruthenium carboxylate catalysts showed only a slight improvement in the selectivity towards 3a (Table 1, entries 3, 5 vs. 2, 4).
Better conversion and selectivity towards the monoarylated product were obtained after 24 h with 5 mol% of RuCl2(PPh3)(p-cymene) (Table 1, entry 6). The replacement of PPh3 by bulkier and more electron donating phosphines such as P(CH2Ph)3, PCy3, Pi-Pr3 or P(o-Me-C6H4)3 did not improve the selectivity of the formation of 3a (Table 1, entries 7–10). Neither steric nor electronic property of the phosphine ligand had a significant positive effect on the selective formation of 3a with respect to PPh3 in water. Noteworthily, the selective formation of 3a could be achieved at 80 °C in 5 h, and even at 60 °C in 16 h (Table 1, entries 11–12). The reaction performed in NMP at 80 °C for 5 h provided only 45% of conversion (entry 11). This reveals that water is a more efficient solvent at lower temperature than NMP for monoarylation.
We performed a kinetic study, in order to better observe the variations of conversion and selectivity as a function of the reaction time with 5 mol% of the RuCl2(PPh3)(p-cymene) catalyst in water. After 1 h, the conversion was only 71% with 99% of selectivity towards the monoarylated product. When the reaction was carried out for 24 h, the selectivity of 3a decreased from 99% to 89%, which showed that the diarylated product was formed during the course of the reaction at the expense of the monoarylated product. We observed that the best formation of monoarylated 2-phenylpyridine 3a was obtained in 3 h (Table S1†). The reaction was performed with various catalysts in 3 h at 100 °C in order to evaluate the influence of various phosphorous and arene ligands coordinated to ruthenium (Tables S2 and S3†). Hence, after the screening of the reaction of 2-phenylpyridine with chlorobenzene it could be concluded that the best conditions to reach the monoarylated product 3a were to use the RuCl2(PPh3)(p-cymene) catalyst: (i) at 80 °C, with 5 mol% of the catalyst with a reaction time of 5 h, or (ii) at 100 °C, with 5 mol% of the catalyst with a reaction time of 3 h.
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Entry | Het-X | T (h) | Convb (%) | M/Dc | Yieldd (%) |
---|---|---|---|---|---|
a Reaction conditions: 0.6 mmol of 2-phenylpyridine, 5 mol% of RuCl2(PPh3)(p-cymene), 3 equiv. of K2CO3, 10 μL of tetradecane (internal standard) for GC, 0.5 mmol of Het-X in 2 mL of water, 80 °C.b Conversion determined by gas chromatography based on (hetero)arylhalide.c M/D ratio determined by gas chromatography.d Isolated yield. | |||||
1 | ![]() | 5 | 98 | 94/6 | ![]() |
2 | ![]() | 8 | 88 | 96/4 | ![]() |
10 | 89 | 96/4 | |||
3 | ![]() | 13 | 90 | 90/10 | ![]() |
14 | 92 | 90/10 | |||
4 | ![]() | 6 | 78 | 96/4 | ![]() |
13 | 99 | 90/10 | |||
5 | ![]() | 6 | 10 | — | |
6 | ![]() | 3 | 96 | 96/4 | ![]() |
4 | 97 | 95/5 | |||
7 | ![]() | 6 | 90 | 90/10 | ![]() |
10 | 96 | 88/12 | |||
8 | ![]() | 8 | 50 | 88/12 | ![]() |
24 | 60 | 80/20 | |||
9 | ![]() | 3 | 100 | 86/14 | ![]() |
4 | 100 | 85/15 | |||
10 | ![]() | 3 | 100 | 89/11 | ![]() |
4 | 100 | 87/13 | |||
11 | ![]() | 3 | 81 | 81/19 | ![]() |
4 | 83 | 80/20 | |||
6 | 100 | 73/22 |
The reaction of 2-phenylpyridine with various electron donating and electron withdrawing heteroarenes was performed. The monophenylated 2-phenylpyridine 3a was obtained by the reaction with phenylchloride in 5 h with 76% isolated yield (Table 2, entry 1). The reaction with arylhalides containing the para substituted electron donating groups, –OMe, –NMe2, gave 69% and 72% yield, respectively in 8–13 h (Table 2, entries 2–3). With the electron withdrawing para CF3-substituted phenylchloride 99% of conversion was obtained in 13 h leading to 80% of monoarylated product 3h (Table 2, entry 4). With 4-methyl chlorobenzoate 2j and 4-chloroacetophenone 2k the reactions were completed in shorter reaction times (3–10 h), providing 83% and 77% of monoarylated products 3j and 3k, respectively (Table 2, entries 6–7). With o-methylchlorobenzene 2l only 30% of product 3l was isolated after 24 h (Table 2, entry 8).
The reaction with heterocyclic halides such as 2-chlorothiophene, 5-methyl-2-chlorothiophene, 6-bromo-2-methylpyridine was performed successfully with short reaction times (Table 2, entries 9–11). With 2b and 2c, the reaction went to completion within 3 h affording 3b and 3c in 76–79% isolated yields, whereas with 2d, only 81% conversion of 2-phenylpyridine was obtained in 3 h, but the complete conversion was obtained in 6 h leading only to 52% of isolated 3d (Table 2, entry 11).
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Entry | Het-X | T (h) | Convb (%) | M/Dc | Yd (%) |
---|---|---|---|---|---|
a Reaction conditions: 0.6 mmol of phenylpyrazole, 5 mol% of RuCl2(PPh3)(p-cymene), 3 equiv. of K2CO3, 10 μL of tetradecane (internal standard) for GC, 0.5 mmol of Het-X in 2 mL of water, 80 °C.b Conversion determined by gas chromatography.c M/D ratio determined by gas chromatography.d Isolated yield. | |||||
1a | ![]() | 7 | 97 | 90/10 | ![]() |
1b | 14 (65 °C) | 62 | 93/7 | ||
2a | ![]() | 5 | 96 | 89/11 | ![]() |
2b | 20 (65 °C) | 98 | 90/10 | ||
3a | ![]() | 5 | 80 | 78/22 | ![]() |
3b | 7 | 84 | 75/25 | ||
20 (65 °C) | 98 | 74/26 | |||
4a | ![]() | 8 | 78 | 84/16 | ![]() |
4b | 24 (65 °C) | 91 | 75/25 |
Similar conditions for selective catalytic monoarylation were used to produce new monoarylated products in water from functional arenes containing already one ortho substituent. As there is no risk to get parasite ortho diarylation the phosphine can be replaced by the carboxylate ligand. Thus the [RuCl2(p-cymene)]2–4 KOPiv catalytic system was applied for the monoarylation of the ortho C–H bond of 2-o-tolylpyridine 1c. Thus the ortho (hetero)arylated derivatives 4e (71%), 4f (60%), 4g (63%), 4h (58%) were obtained by direct arylation with chlorobenzene, and the heterocyclic halides 2b, 2c and 2d (Scheme 1).
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Scheme 1 Selective monoarylation of 2-o-tolylpyridine with (hetero)arylhalides in water. (a) Reaction conditions: 0.5 mmol of 2-o-tolylpyridine, 5 mol% of [RuCl2(p-cymene)]2, 20 mol% of KOPiv, 3 equiv. of K2CO3, 10 μL of tetradecane (internal standard) for GC, 1.25 mmol of aryl(hetero)halide in 2 mL of water. (b) Conversion determined by gas chromatography. (c) Isolated yield. |
The monoheteroarylated derivative 3j was first obtained from the monoarylation of phenylpyridine with 4-chlorobenzoate in water in the presence of RuCl2(PPh3)(p-cymene) (Table 2). The reaction of 3j with 2-chlorothiophene was then performed in the presence of RuCl2(PPh3)(p-cymene) in water for 20 h to give only 70% of conversion. Then the same reaction in the presence of Ru(OAc)2(p-cymene) or Ru(OPiv)2(p-cymene)7 was carried out at 120 °C and provided the mixed diarylated product with 99% conversion in 20 h and afforded 77% isolated yield of 7 (Scheme 2). For comparison, when the same reaction with 3j was performed in NMP as a solvent, only 20% conversion was obtained after 20 h. The advantage of using water as a solvent medium was obvious as water not only acts as a solvent but also enhances the rate of the reaction for the formation of unsymmetrical or mixed diarylated products.
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Scheme 2 Successive arylations in water and preparation of difunctional unsymmetrical diarylated arenes. Reaction conditions: 0.25 mmol of monoarylated heteroarenes, 5 mol% of Ru(OAc)2(p-cymene), 3 equiv. of K2CO3, 10 μL of tetradecane (internal standard) for GC, 0.5 mmol of Het-X in 1.5 mL of water. (a) Conversion determined by gas chromatography. (b) Isolated yield. |
The transformation in water of 3j with 4-chloroacetophenone provided the mixed ketone carboxylate product 8 isolated in 71% yield after 24 h. Similarly, the monoarylated pyrazole 5j was reacted in water with 2-chlorothiophene and 4-chloroacetophenone. After 24 h the unsymmetrical diarylated products 9 and 10 were isolated in 72 and 83% yields.
![]() | (4) |
However it was recently established that arenes containing a nitrogen directing group were successfully alkenylated with a carboxylate-ruthenium(II) catalyst but in acetic acid.9 The alkenylation of monoarylated product 5j with n-butyl acrylate was attempted using these conditions in the presence of Ru(OAc)2(p-cymene) as a catalyst with Cu(OAc)2·H2O as an oxidant in AcOH at 100 °C during 24 h. The difunctional mixed aryl alkenylheteroarene 11 was thus successfully isolated in 43% yield (eqn (4)).
Footnote |
† Electronic supplementary information (ESI) available: Experimental procedures, spectroscopic and analytical data. See DOI: 10.1039/c2gc36222h |
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