Synthesis of m-Aryloxy Phenols: Comparison
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Innovative synthetic methods have been developed for the preparation of m-aryloxy phenols, which has allowed for the preparation of complex m-aryloxy phenols with functional groups, such as esters, nitriles, and halogens, that impart specific properties of these compounds.

  • m-aryloxy phenols
  • potential biological activities
  • hydroxylation of benzenes

1. Introduction

m-Aryloxy phenols have a wide range of applications, including as antioxidants, ultraviolet absorbers, and flame retardants. They are commonly used in the production of plastics, adhesives, and coatings due to their ability to improve these materials’ thermal stability and flame resistance. In addition, m-aryloxy phenols have been found to have potential biological activities, including anti-tumor and anti-inflammatory effects [1].
Phenol derivatives have been widely researched, as they have high potential for synthesizing bioactive natural products and conducting polymers. Many synthesis methods have been developed for phenol derivatives, with conventional strategies focusing on functionalizing and transforming functional groups around the aromatic ring. These strategies include selective hydroxylation of benzenes, nucleophilic and electrophilic aromatic substitutions, and metal-catalyzed cross-coupling reactions [2].
The most successful synthesis strategies were developed based on the Ullmann copper-mediated aromatic nucleophilic substitution reactions, which were reported in the early 1900s by Fritz Ullmann and Irma Goldberg. In the original Ullmann reaction protocol, stoichiometric amounts of copper salt were used, along with high reaction temperatures (≥200 °C) and prolonged reaction times. However, the modern variants of the Ullmann reaction have focused on using copper-mediated (stoichiometric or catalytic) reactions between aryl halides and other reagents, such as amines, phenols, or thiophenols, to produce aryl-amine, -ether, or -thioether compounds, respectively (Scheme 1) [3][4].
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Scheme 1. Schematic representation of the Ullmann reaction and Ullmann condensation.
Despite the expanded scope of the Ullmann reaction, the term primarily refers to the copper-catalyzed synthesis of biaryls from aryl halides. This protocol has been widely adopted due to its high efficiency and versatility in constructing complex biaryl compounds. The Ullmann reaction remains an essential tool in modern organic synthesis and has contributed significantly to the development of many natural products, pharmaceuticals, and materials [5].
Although nucleophilic aromatic substitution is a highly effective method for synthesizing phenol derivatives, the strong influence of the hydroxyl group on ortho/para substitution makes it difficult to prepare meta-substituted phenol derivatives.
The synthesis of m-aryloxy phenols is a significant area of research, as it allows for the preparation of new compounds with tailored properties and applications. In light of their unique properties and broad range of applications, m-aryloxy phenols represent an important area of research with significant potential for future developments.

2. Synthesis of m-Aryloxy Phenols by Demethylation of m-Methoxy Phenols

The demethylation reaction involves the elimination of a methyl group from a molecule. One example of this reaction is the demethylation of m-methoxy phenols, which forms m-aryloxy phenols. There exist multiple approaches for demethylation, including chemical and catalytic methods. The most prevalent chemical method involves the utilization of potent acids, such as sulfuric acid, hydrochloric acid, or nitric acid. These acids convert the methoxy group into a hydroxyl group [6]. In contrast, catalytic demethylation methods usually use transition metal catalysts, including copper or palladium. These methods can be employed through various mechanisms, including hydrogenation, transfer hydrogenation, and activation of C-H bonds. The use of hydrogen bromide and boron tribromide (BBr3) as catalysts in demethylation reactions represents a valuable approach for the synthesis of m-aryloxy phenols. Bronsted acid HBr and Lewis acid BBr3 can coordinate with electron-rich sites in organic compounds and enhance the outcome of organic reactions. This property enables the efficient demethylation of methoxy phenols to m-aryloxy phenols [7][8]. In Kormos and his team’s research, 4-(3-hydroxyphenoxy) benzoic acid was synthesized from 4-(3-methoxyphenoxy) benzoic acid by refluxing it with 48% hydrogen bromide in acetic acid. By condensing the 4-(3-hydroxyphenoxy) benzoic acid with piperazine using N-ethylcarbodiimide hydrochloride (EDC·HCl) and a catalytic hydroxy benzotriazole (HOBt), the team synthesized N-(1S)-1-{[(3S)-4-(3-hydroxyphenyl)-3-methylpiperazin-1-yl]-methyl}-2-methylpropyl-4-(3-hydroxyphenoxy) benzamide (Scheme 2) [9].
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Scheme 2. Synthesis of 4-(3-hydroxyphenoxy) benzoic acid and its derivative with piperazine amine.
This compound showed strong antagonistic properties at the κ opioid receptor, with inhibition agonist-stimulated [35S]GTPγS binding in cloned human μ (DAMGO) -Ke(nM)a = 69 ± 14, δ (DPDPE) − Ke(nM)a = 625 ± 120, and κ (U69,593) − Ke(nM)a = 1.85 ± 0.51. The authors believed these compounds will be useful in the development of clinical candidates for treating conditions such as depression, anxiety, schizophrenia, and addictions, as well as serving as pharmacological tools [9][10][11]. In 2022, Yamamoto et al. reported the synthesis of N-(2-(3-hydroxyphenoxy)-4-nitrophenyl)methanesulfonamide through the demethylation of the corresponding methoxy derivatives by utilizing BBr3 as a dealkylating agent (Scheme 3). The resulting compound was utilized to synthesize isomeric [11C] methoxy analogs of nimesulide as a suitable radiotracer candidate for imaging the expression of Cyclooxygenase-2 (COX-2) in the brain. COX-2 expression has been documented in various tumor types, including head and neck cancers, colorectal cancers, and melanomas [12][13].
Molecules 28 02657 sch003 550
Scheme 3. Synthesis of N-(2-(3-hydroxyphenoxy)-4-nitrophenyl)methanesulfonamide.

3. Synthesis of aryloxy phenols by reaction between aryl halides and resorcinol

The reaction between aryl halides and resorcinol involves a nucleophilic aromatic substitution mechanism. In this mechanism, resorcinol undergoes deprotonation under basic conditions and subsequently acts as a nucleophile on the aromatic ring of the aryl halide. This results in the formation of an intermediate, in which the nucleophile attacks the ring, leading to the substitution of the halide group. The intermediate species contains an oxide anion, which is formed due to the loss of a proton. The final product of the reaction is an aryloxy phenol, which can be obtained in good yield under appropriate reaction conditions [14].

In 2010, Vagin and colleagues published a study detailing the synthesis of 5-(3-hydroxyphenoxy)-2-nitroaniline from 5-chloro-2-nitroaniline and resorcinol. The reaction was performed using sodium hydride as a base and DMF as a solvent and was carried out under an argon atmosphere by heating the reaction mixture at 125°C for 24 hours. They then used a hydrogenation reaction with a Pd/C catalyst to obtain 4-(3-hydroxyphenoxy)-1,2-benzyldiamine (Scheme 4)  [15].

4. Sonogashira Coupling: A Copper-Catalyzed Method for Biaryl Synthesis

The Sonogashira coupling reaction represents a variation of cross-coupling, wherein the interaction between aryl boronic acids and phenols is facilitated by the presence of a copper catalyst and a base. Copper (II) acetate (Cu(OAc)2) serves as a typical example of a copper catalyst for this reaction, while potassium carbonate (K2CO3) is commonly used as the base. The reaction mechanism involves the formation of a complex between the copper and phenol, which subsequently reacts with the aryl boronic acid to form an intermediate. This intermediate undergoes transmetallation to furnish the final biaryl product. Due to its high efficiency and versatility, the Sonogashira coupling reaction has gained widespread use in the synthesis of pharmaceuticals and agrochemicals, among other applications[16][17].

The report by Bryan and colleagues in 2015 summarizes research endeavors centered on forming new carbon-heteroatom bonds using organoboron reagents through copper acetate-mediated reactions under ultrasound irradiation. The methodology involves incorporating ultrasound irradiation in the Chan-Evans-Lam reaction to achieve the O-arylation of phenols, N-arylation of anilines and indoles, and S-arylation of thiols. The utilization of ultrasound irradiation was discovered to significantly reduce reaction times from 72 hours to 4 hours while increasing product yields by an average of 20% [18].

5. Synthesis of m-Aryloxy phenols using Grignard Reagents

The utilization of Grignard reagents, a type of organometallic compound, in the synthesis of aryloxy phenols via reaction with aldehydes or ketones has received widespread attention in the field of organic chemistry. Through interaction with a carbonyl compound, a complex intermediate is formed, which upon treatment with acidic conditions, gives rise to the corresponding alcohol. The alcohol can then be oxidized through the use of oxidation reagents such as hydrogen peroxide (H2O2) or sodium hypochlorite (NaClO) to produce the desired aryloxy phenol.

It is important to note that the reaction conditions, such as the choice of solvent and the presence of catalysts or bases, have a significant impact on the reactivity, selectivity, yield, and stereochemistry of the Grignard reaction and the final product [19].

In 2012, researchers led by Pidathala used 4-(3-methoxyphenoxy)benzaldehyde in a Grignard reaction to produce an intermediate alcohol.

6. Hydrolysis of Diazonium Salts Using a Two-Phase System

In 2015, Taniguchi et al. published findings on the synthesis of 3-phenoxyphenol and 3-(4-nitrophenoxy)phenol. The method involved the hydrolysis of intermediate diazonium salts derived from anilines in a two-phase system of cyclopentyl methyl ether (CPME) and water, resulting in high yields of the desired compounds. These products were found to be key components for the production of raw materials for functional plastics, specifically polyimide resin [20].

7. Synthesis of 3-aryloxyphenols from 3-chlorocyclohex-2-en-1-one

In 2023, a chemical reaction was reported by Clive's group wherein 3-chlorocyclohex-2-en-1-one was treated with phenols in the presence of K2CO3 resulting in the formation of 3-(aryloxy)cyclohex-2-en-1-ones . The synthesized products were then subjected to bromination at the C(2) position using NBS in DMF, ultimately forming the brominated products. Subsequently, the brominated compounds were aromatized to form 3-(aryloxy)phenols through treatment with DBU in PhMe or MeCN. This multi-step reaction sequence necessitated the use of several reagents and conditions to generate the final compounds. The method presently utilized operates at ambient temperature, and does not employ any heavy metals or ligands. Moreover, it circumvents the procedural steps required to overcome the o,p-directing effect of oxygen, owing to the readily available 1,3-functional group relationship inherent in the starting material, namely cyclohexane-1,3-dione [21].

8. Conclusion

In summary, the past decade has witnessed remarkable advances in the synthesis and utilization of m-aryloxy phenols. The implementation of various synthetic methodologies has resulted in the preparation of structurally diverse m-aryloxy phenols, including biologically active compounds with promising pharmacological applications. Moreover, m-aryloxy phenols have demonstrated versatility in the fields of materials science and organic electronics. These achievements have propelled further research towards the synthesis, characterization, and application of m-aryloxy phenols, and it is anticipated that this research area will continue to expand in the foreseeable future. The growing interest in m-aryloxy phenols underscores their potential to emerge as key compounds in the field of synthetic organic chemistry and their relevance to a diverse range of technological applications.

References

  1. Latha, G.; Devarajan, N.; Karthik, M.; Suresh, P. Nickel-Catalyzed Oxidative Hydroxylation of Arylboronic Acid: Ni(HBTC)BPY MOF as an Efficient and Ligand-Free Catalyst to Access Phenolic Motifs. Catal. Commun. 2020, 136, 105911.
  2. Wang, S.K.; Chen, M.T.; Zhao, D.Y.; You, X.; Luo, Q.L. Iodine-Catalyzed Oxidative Aromatization: A Metal-Free Concise Approach to meta-Substituted Phenols from Cyclohex-2-enones. Adv. Synth. Catal. 2016, 358, 4093–4099.
  3. Ullmann, F. Ueber eine neue Bildungsweise von Diphenylaminderivaten. Ber. Der Dtsch. Chem. Ges. 1903, 36, 2382–2384.
  4. Ullmann, F. Ueber eine neue Darstellungsweise von Phenyläthersalicylsäure. Ber. Der Dtsch. Chem. Ges. 1904, 37, 853–854.
  5. Hassan, J.; Sévignon, M.; Gozzi, C.; Schulz, E.; Lemaire, M. Aryl-aryl Bond Formation One Century after the Discovery of the Ullmann Reaction. Chem. Rev. 2002, 102, 1359–1470.
  6. Zuo, L.; Yao, S.; Wang, W.; Duan, W. An Efficient Method for Demethylation of Aryl Methyl Ethers. Tetrahedron Lett. 2008, 49, 4054–4056.
  7. Bradsher, C.K.; Brown, F.C.; Porter, H.K. Synthesis and Fungistatic Activity of Some 3-Hydroxybiphenyl Derivatives. J. Am. Chem. Soc. 1954, 76, 2357–2362.
  8. McOmie, J.F.W.; Watts, M.L.; West, D.E. Demethylation of Aryl Methyl Ethers by Boron Tribromide. Tetrahedron 1968, 24, 2289–2292.
  9. Kormos, C.M.; Jin, C.; Cueva, J.P.; Runyon, S.P.; Thomas, J.B.; Brieaddy, L.E.; Mascarella, S.W.; Navarro, H.A.; Gilmour, B.P.; Carroll, F.I. Discovery of N--4-phenoxybenzamide analogues as selective kappa opioid receptor antagonists. J. Med. Chem. 2013, 56, 4551–4567.
  10. Carroll, F.I.; Carlezon Jr, W.A. Development of κ Opioid Receptor Antagonists. J. Med. Chem. 2013, 56, 2178–2195.
  11. Puls, K.; Olivé-Marti, A.L.; Pach, S.; Pinter, B.; Erli, F.; Wolber, G.; Spetea, M. In Vitro, In Vivo and In Silico Characterization of a Novel Kappa-Opioid Receptor Antagonist. Pharmaceuticals 2022, 15, 680.
  12. Yamamoto, Y.; Tago, T.; Toyohara, J.; Saito, Y.; Yamamoto, F. Radiosynthesis and in Vivo and ex Vivo Evaluation of Isomeric methoxy Analogs of Nimesulide as Brain Cyclooxygenase-2-Targeted Imaging Agents. Biol. Pharm. Bull. 2022, 45, 94–103.
  13. Yamamoto, Y.; Hisa, T.; Arai, J.; Saito, Y.; Yamamoto, F.; Mukai, T.; Ohshima, T.; Maeda, M.; Ohkubo, Y. Isomeric Methoxy Analogs of Nimesulide for Development of Brain Cyclooxygenase-2 (COX-2)-Targeted Imaging Agents: Synthesis, In Vitro COX-2-Inhibitory Potency, and Cellular Transport Properties. Bioorg. Med. Chem. 2015, 23, 6807–6814.
  14. Lindley, J. Copper Assisted Nucleophilic Substitution of Aryl Halogen. Tetrahedron 1984, 40, 1433–1456. [Google Scholar] [CrossRef]
  15. Vagin, S.I.; Reichardt, R.; Klaus, S.; Rieger, B. Conformationally flexible dimeric salphen complexes for bifunctional catalysis. J. Am. Chem. Soc. 2010, 132, 14367–14369.
  16. Thomas, A.M.; Sujatha, A.; Anilkumar, G. Recent Advances and Perspectives in Copper-Catalyzed Sonogashira Coupling Reactions. RSC Adv. 2014, 4, 21688–21698.
  17. Min, H.; Palani, T.; Park, K.; Hwang, J.; Lee, S. Copper-Catalyzed Direct Synthesis of Diaryl 1, 2-Diketones from Aryl Iodides and Propiolic Acids. J. Org. Chem. 2014, 79, 6279–6285.
  18. Bryan, J.M.; George, W.K. Copper mediated formation of carbon-heteroatom bonds using organoboron reagents and ultrasound. Heterocycles Int. J. Rev. Commun. Heterocycl. Chem. 2015, 90, 271–297.
  19. Mann, F.G.; Stewart, F.H. The Action of Magnesium and of Grignard Reagents on Certain Benzyl Ethers. Part I. The Action of Magnesium on o-, m-, and p-Alkoxy-and-phenoxy-methylbenzyl Chlorides. J. Chem. Soc. 1954, 2826–2832.
  20. Taniguchi, T.; Imoto, M.; Takeda, M.; Nakai, T.; Mihara, M.; Iwai, T.; Ito, T.; Mizuno, T.; Nomoto, A.; Ogawa, A. Hydrolysis of Diazonium Salts Using a Two-Phase System (CPME and Water). Heteroat. Chem. 2015, 26, 411–416.
  21. Duvvuru, B.; Amankulova, D.; Gauden, S.; Haffemayer, T.; Clive, D.L. A mild alternative to the classical Ullmann coupling for preparation of 3-aryloxy phenols. Tetrahedron 2023, 133, 133264.
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