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Communication

Electrochemical Synthesis of 1,1′-Binaphthalene-2,2′-Diamines via Transition-Metal-Free Oxidative Homocoupling

by
Duona Fan
,
Md. Imrul Khalid
,
Ganesh Tatya Kamble
,
Hiroaki Sasai
and
Shinobu Takizawa
*
SANKEN, Osaka University, Suita Campus, Mihogaoka, Ibaraki-shi, Osaka 567-0047, Japan
*
Author to whom correspondence should be addressed.
Sustain. Chem. 2022, 3(4), 551-557; https://doi.org/10.3390/suschem3040034
Submission received: 29 October 2022 / Revised: 29 November 2022 / Accepted: 1 December 2022 / Published: 4 December 2022
(This article belongs to the Topic Green and Sustainable Chemistry)
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Abstract

:
The facile and green synthesis of 1,1′-binaphthalene-2,2′-diamine (BINAM) derivatives was established via the anodic dehydrogenative homo-coupling of 2-naphthylamines. The sustainable protocol provided a series of BINAMs in excellent yields of up to 98% with good current efficiency (66%) and H2 as the sole coproduct without utilizing transition-metal reagents or stoichiometric oxidants.

1. Introduction

1,1′-Bi-2-naphthylamine (BINAM) and its derivatives are widely used as building blocks for transition-metal ligands and organocatalysts [1,2,3,4], as well as chiroptical materials for fluorescence sensing [5,6,7]. Among their syntheses, transition-metal mediated coupling of 2-naphthylamine derivatives has been well established [8,9,10,11,12]. In particular, the Ullmann [13] and metal-mediated C(sp2)–H oxidative [14,15,16,17,18,19,20] coupling reactions of 2-naphthylamines are the most popular synthetic approaches to obtaining BINAMs. Benzidine rearrangement [21,22,23] and Smiles rearrangement of phenolic compounds [24] have been reported to be alternative synthetic methods for BINAMs. However, the regio- and chemoselective C–C coupling of 2-naphthylamines remains challenging, probably because these strategies require the use of excess amounts of metals and oxidants, which leads to many side reactions of starting material and over-oxidation of coupling products.
Biaryls synthesis through anodic oxidation utilizing electrochemical synthesis has emerged as a promising green and sustainable approach over the last few decades. The electrochemical dehydrogenative coupling of aryls utilizes electricity as an alternative to oxidants and produces H2 as the sole coproduct without generating any toxic waste; thus, this approach exhibits great advantages in terms of high atom economy and environmentally benign synthesis protocols [25,26]. Although remarkable achievements have been made in the electrochemical dehydrogenative heterocoupling of anilines [27], few reports on the homocoupling of aniline derivatives [28,29], particularly 2-naphthylamines, are available. In the 1980s, Gossage [30] and Sereno [31] independently described the electrochemical dehydrogenative homocoupling of 2-naphthylamines, which afforded BINAMs, but in low yield. Thus, the development of efficient oxidative homocoupling protocols for 2-naphthylamines via electrochemical synthesis is of great importance.
Because the discharge of the electrolyte or solvent leads to a low yield and poor current efficiency, we reexamined the anodic dehydrogenative homocoupling conditions of 2-naphthylamines to save energy and chemical loading in the pursuit of developing environmentally benign chemical reactions. To our delight, under the newly established conditions, the corresponding homocoupling products were obtained in 98% yield with good current efficiency (66%; Scheme 1).

2. Materials and Methods

2.1. Materials

N-Phenyl-2-napthylamine (1a) was purchased from Tokyo Chemical Industries (TCI). All commercially available organic and inorganic compounds were used directly without further purification.

2.2. Methods

2.2.1. Spectroscopy and Spectrometry

1H- and 13C-NMR spectra were recorded at 25 °C using a JEOL JMN ECS400 FT NMR instrument (1H-NMR 400 MHz; 13C-NMR 100 MHz). The 1H-NMR spectra are reported as follows: chemical shift in ppm downfield of tetramethylsilane and referenced to a residual solvent peak (CHCl3) at 7.26 ppm, integration, multiplicities (s = singlet, d = doublet, t = triplet, q = quartet, m = multiplet), and coupling constants (Hz). The 13C-NMR spectra are reported in ppm relative to the central line of the triplet for CDCl3 at 77.16 ppm. ESI-MS spectra were obtained using a JMS-T100LC instrument (JEOL). FT-IR spectra were recorded using a JASCO FT-IR system (FT/IR4100). Thin-layer chromatography (TLC) analysis of the reaction mixture was performed on Merck silica gel 60 F254 TLC plates and visualized under UV light. Column chromatography on SiO2 was performed using Kanto Silica Gel 60 (63–210 μm).

2.2.2. General Protocol for the Anodic Homocoupling of 2-Naphthylamines

ElectraSyn 2.0 and platinum were utilized as the reaction device and electrode, respectively. A suspension of 2-naphthylamines (0.1 mmol) and nBu4NPF6 (0.1 M) in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) (5 mL) was added to an undivided vessel and stirred under a constant current of 4 mA for 2 h. The electrolyte was removed using short silica gel column chromatography (nhexane/ethyl acetate = 1/1). The fraction was dried, and the crude product was purified by silica-gel column chromatography (nhexane/ethyl acetate = 20/1) to afford the pure homocoupling product.

3. Results

3.1. Optimization of the Reaction Conditions

Initially, we screened the electrodes, solvent systems, currents, and electrolytes to determine the optimal conditions (Table 1, also see supporting information). The electrodes were screened by employing 0.1 mmol N-phenyl-2-naphthylamine (1a, oxidative potential 1.05 eV; see Supporting Information) as the model substrate. The platinum electrode exhibited good reactivity, affording homocoupling product 2a in 98% yield (current efficiency, 66%) without the formation of any side product (entry 1). In contrast, the carbon–platinum [32] and fluorine-doped tin oxide(FTO) [33] electrodes gave 2a in 43% and 29% yields, respectively, with low current efficiencies (entries 2 and 3). Other alcoholic reaction solvents, such as methanol, ethanol, and trifluoroethanol, reduced the yield of 2a to 6–12% with current efficiencies of 4–8% (entries 4–6), along with a 5% yield of aza [5] helicene. HFIP, an appropriate solvent for the reaction, serves as an excellent hydrogen bond donor and provides highly persistent radical cations [34,35]. The effect of a constant current was also investigated. As shown in entry 7, when a current of 2 mA was employed for the electrosynthesis process, the current efficiency increased to 80%, but the yield of 2a decreased to 60%. In contrast, employing a current of 6 mA for the electrosynthesis process led to the formation of 2a in 49% yield, with a current efficiency of 22% (entry 8). Suppressing the discharge of the electrolyte or solvent resulted in higher yield and current efficiency. Among the electrolytes we screened, nBu4NPF6 proved to be superior to LiClO4 (2a, 57% yield due to low solubility in HFIP) and nBu4NClO4 (2a, 29% yield) (entries 9 and 10). No reaction occurred in the absence of electricity (entry 11).

3.2. Scope of Substrates

With the optimized conditions in hand (reaction solvent: HFIP, electrolyte: nBu4NPF6 (0.1 M), electrode: platinum, constant current: 4 mA, and reaction temperature: 25 °C), we investigated the substrate scope of the 2-naphthylamines (Figure 1). The electrochemical homocoupling of 2-naphthylamines 1 proceeded smoothly at moderate current efficiencies (44–66%). N-Phenyl-2-naphthylamine (1a) produced homocoupling product 2a in 98% yield. N-4-Tolyl and N-2-tolyl-2-naphthylamines (1b and 1c), respectively, were also found to be appropriate coupling precursors, giving the corresponding homocoupling products 2b and 2c in 92% and 83% yields, respectively. The reaction of substrates 1d and 1e with electron-donating or electron-withdrawing groups, such as N-2,3-dimethoxyphenyl and N-4-bromophenyl, on the nitrogen atom, showed good functional group tolerance, giving binaphthylamines 2d and 2e in good yields. When N-(1,1′-biphenyl)-4-yl-2-naphthylamine (1f) was used as the substrate, a moderate yield of the coupling product 2f was obtained because of the poor solubility of 1f in HFIP. The reactions of N-alkyl-2-naphthylamines, such as N-methyle-2-naphthylamine (1g), N-ethyl-2-naphthylamine (1h), N-isopropyl-2-naphthylamine (1i), and N-t-butyle-2-naphthylamine (1j) afforded the corresponding homocoupling products 2g, 2h, 2i and 2j in 30%, 87%, 85% and 72% yields, respectively. The dehydrogenative coupling reactions of N-aryl-2-naphthylamines (1k–1n) with various substituents were also conducted. Products 2k and 2l with methoxy groups 2m and 2n with phenyl and cyano groups were readily obtained in good to excellent yields (65–95% yields). N-Naphthyl-2-naphthyl amine (1o) could not be tolerated. Finally, N-benzyl-naphthylamine (1p) was employed in the electrochemical homocoupling reaction. The corresponding product 2p was obtained an 85% yield and could be transformed into BINAM with Lewis acid (See Supporting Information).

4. Discussion

In our study, the homocoupling reaction of 2-naphthylamines proceeded smoothly with good current efficiency. To further understand the relevant mechanism, we conducted the heterocoupling reactions of 1b with N-4-tolyl (an electron-donating group) and 1e with N-4-bromo-phenyl (an electron-withdrawing group) under the optimal conditions (Scheme 2).
Homocoupling product 2b was obtained in 90% yield as the major product, along with homocoupling product 2e in 10% yield and trace amounts of heterocoupling product 2be. The relative proportions of the products arising from the radical–radical coupling reactions are aligned with their relative reactivities [36,37,38]. In principle, 1e is less oxidizable than 1b, which should result in the formation of homocoupling 2b as the major product. The results support our hypothesis that the present coupling reaction of 1 proceeds through radical–radical coupling, as shown in Scheme 3. Triggering by single-electron transfer (SET) of 1a on the anode made the formation of intermediate I. The generated I species could be in equilibrium into Ia and Ib by electron transfer. Then a radical–radical coupling of Ib proceeded to afford the coupling product 2b through the oxidation of intermediate II. On the cathode, the generated H+ was reduced to give H2 as a sole coproduct.

5. Conclusions

We developed a facile and sustainable protocol for the homocoupling of various 2-naphthylamines with up to 98% yield and good current efficiency (66%). This new protocol not only saves energy and chemical loading but also significantly improves the product yield, thus representing a significant improvement to the previous electrosynthesis approach. Investigations of the further applications of homocoupling products are ongoing in our laboratory.

Supplementary Materials

The supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/suschem3040034/s1; Figure S1: IKA device ElectraSyn 2.0 standard setup; Table S1. Screening solvent of constant current for optimizing reaction conditions; Figure S2: CV experiments (MeCN) as a solvent with Bu4NPF6 (0.1 M) as an electrolyte.

Author Contributions

S.T. and H.S.: conceptualization, resources, writing—reviewing, and editing. D.F.: investigation, resources, visualization, validation, writing—original draft. M.I.K., and G.T.K.: investigation, resources, and validation. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by JSPS KAKENHI Grant Numbers 22K06502 in Grant-in-Aid for Scientific Research (C), Transformative Research Areas (A) 21A204 Digitalization-driven Transformative Organic Synthesis (DigiTOS), 22KK0073 in Fund for the Promotion of Joint International Research (Fostering Joint International Research (B)) from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT), and the Japan Society for the Promotion of Science (JSPS), JST CREST (No. JPMJCR20R1), and Hoansha Foundation.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data available in a publicly accessible repository.

Acknowledgments

We acknowledge the technical staff of the Comprehensive Analysis Center of SANKEN, Osaka University (Japan).

Conflicts of Interest

The authors declare no conflict of interest.

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Suschem 03 00034 sch001 550
Scheme 1. Electrochemical dehydrogenative homocoupling of 2-naphthylamines.
Scheme 1. Electrochemical dehydrogenative homocoupling of 2-naphthylamines.
Suschem 03 00034 sch001
Suschem 03 00034 g001 550
Figure 1. Substrate scope of N-naphthylamines a–d.
Figure 1. Substrate scope of N-naphthylamines a–d.
Suschem 03 00034 g001
Suschem 03 00034 sch002 550
Scheme 2. Electrochemical heterocoupling of substrate 1b and 1e.
Scheme 2. Electrochemical heterocoupling of substrate 1b and 1e.
Suschem 03 00034 sch002
Suschem 03 00034 sch003 550
Scheme 3. Proposed mechanism for the homocoupling of 2-naphthylamines.
Scheme 3. Proposed mechanism for the homocoupling of 2-naphthylamines.
Suschem 03 00034 sch003
Table
Table 1. Optimization of the conditions for the electrochemical homocoupling of 2-naphthylamines using 1a as the model substrate.
Table 1. Optimization of the conditions for the electrochemical homocoupling of 2-naphthylamines using 1a as the model substrate.
Suschem 03 00034 i001
EntryVariation from Standard Conditions% Yield (% Current Efficiency) a
2a3a
1None99, 98 b (66)-
2C (+)/Pt (−)43 (29)-
3FTO (−)/FTO c (+)29 (20)-
4MeOH instead of HFIP10 (7)5
5EtOH instead of HFIP6 (4)5
6CF3CH2OH instead of HFIP12 (8)-
72 mA60 (80)-
86 mA49 (22)-
9with LiClO4 instead of nBu4NPF657 d (38)-
10with nBu4NClO4 instead of nBu4NPF629 (19)-
11No electricityNo reaction
a NMR yield; b Isolated yield; c FTO = Fluorine-doped tin oxide; d HFIP:MeOH (3:2) for 8 h.
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MDPI and ACS Style

Fan, D.; Khalid, M.I.; Kamble, G.T.; Sasai, H.; Takizawa, S. Electrochemical Synthesis of 1,1′-Binaphthalene-2,2′-Diamines via Transition-Metal-Free Oxidative Homocoupling. Sustain. Chem. 2022, 3, 551-557. https://doi.org/10.3390/suschem3040034

AMA Style

Fan D, Khalid MI, Kamble GT, Sasai H, Takizawa S. Electrochemical Synthesis of 1,1′-Binaphthalene-2,2′-Diamines via Transition-Metal-Free Oxidative Homocoupling. Sustainable Chemistry. 2022; 3(4):551-557. https://doi.org/10.3390/suschem3040034

Chicago/Turabian Style

Fan, Duona, Md. Imrul Khalid, Ganesh Tatya Kamble, Hiroaki Sasai, and Shinobu Takizawa. 2022. "Electrochemical Synthesis of 1,1′-Binaphthalene-2,2′-Diamines via Transition-Metal-Free Oxidative Homocoupling" Sustainable Chemistry 3, no. 4: 551-557. https://doi.org/10.3390/suschem3040034

APA Style

Fan, D., Khalid, M. I., Kamble, G. T., Sasai, H., & Takizawa, S. (2022). Electrochemical Synthesis of 1,1′-Binaphthalene-2,2′-Diamines via Transition-Metal-Free Oxidative Homocoupling. Sustainable Chemistry, 3(4), 551-557. https://doi.org/10.3390/suschem3040034

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