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Synthesis of Bromo Eugenol Derivatives with Molecular Bromine

Department of Chemistry, Faculty of Mathematics and Natural Sciences, IPB University, Bogor, Indonesia

Received: 6 Mar 2024; Revised: 30 May 2024; Accepted: 3 Jun 2024; Published: 30 Jun 2024.
Open Access Copyright 2024 Jurnal Kimia Sains dan Aplikasi under http://creativecommons.org/licenses/by-sa/4.0.

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Abstract
The bromination of eugenol using molecular bromine (Br2) has been widely reported. However, the outcomes have been inconsistent, and as a result, the specific steps of the bromination process have not been definitively established. This research aims to synthesize various derivatives of bromo eugenol, incorporating bromine atoms either in the alkene group, the aromatic ring, or both. The synthetic approaches employed include: (1) direct bromination of eugenol using 1.2, 2.4, and 3.6 equivalents (equiv) of Br2 in chloroform, (2) bromination of eugenyl benzoate with 2.4 equiv of Br2 in chloroform, and (3) debromination of the 1,2-dibromide functionality in selected bromination products using an excess of zinc in ethanol. The bromination steps of eugenol were then proposed based on the composition of the products obtained. Alkene bromination of eugenol predominated with 1.2 equiv of Br2, followed by aromatic bromination with excess Br2 (2.4 and 3.6 equiv). Aromatic substitution primarily occurred at position 6 (ortho to the hydroxyl group) and subsequently at position 5 (para to the methoxy group). Based on these results, we propose that the bromination of eugenol with Br2 proceeds initially through electrophilic addition to the alkene group, followed by electrophilic substitution on the aromatic ring. Protection of the phenol as a benzoyl ester shifted the regioselectivity of the first aromatic bromination from position 6 to 5. Furthermore, the 1,2-dibromide group has been successfully removed by zinc, resulting in derivatives containing bromine atoms only at the aromatic ring. This is by far the first comprehensive report on the bromination of eugenol with Br2 and the first one reporting the bromination of alkene as the main route of bromination with a nearly equimolar amount of Br2.
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Keywords: addition; bromination; eugenol; debromination; substitution

Article Metrics:

  1. Food and Agriculture Organization, Food and agriculture data: crops 2023
  2. Diego Francisco Cortés-Rojas, Claudia Regina Fernandes de Souza, Wanderley Pereira Oliveira, Clove (Syzygium aromaticum): a precious spice, Asian Pacific Journal of Tropical Biomedicine, 4, 2, (2014), 90-96 https://doi.org/10.1016/S2221-1691(14)60215-X
  3. Mamilla R. Charan Raja, Varsha Srinivasan, Sharmila Selvaraj, Santanu Kar Mahapatra, Versatile and Synergistic Potential of Eugenol: A Review, Pharmaceutica Analytica Acta, 6, 5, (2015), 1-6 https://doi.org/10.4172/2153-2435.1000367
  4. Teodoro S. Kaufman, The Multiple Faces of Eugenol. A Versatile Starting Material and Building Block for Organic and Bio-Organic Synthesis and a Convenient Precursor Toward Bio-Based Fine Chemicals, Journal of the Brazilian Chemical Society, 26, 6, (2015), 1055-1085 https://doi.org/10.5935/0103-5053.20150086
  5. Daniel A. Heredia, Enrique L. Larghi, Teodoro S. Kaufman, A Straightforward Synthesis of 5-Methylaaptamine from Eugenol, Employing a 6π-Electrocyclization Reaction of a 1-Azatriene, European Journal of Organic Chemistry, 2016, 7, (2016), 1397-1404 https://doi.org/10.1002/ejoc.201501566
  6. José C. Espinoza-Hicks, Gerardo Zaragoza-Galán, David Chávez-Flores, Víctor H. Ramos-Sánchez, Joaquín Tamariz, Alejandro A. Camacho-Dávila, A Convergent Total Synthesis of the Biologically Active Benzo­furans Ailanthoidol, Egonol and Homoegonol from Biomass-Derived­ Eugenol, Synthesis, 50, 17, (2018), 3493-3498 https://doi.org/10.1055/s-0037-1610169
  7. Santiago J. Bolivar Ávila, Gabriela N. Ledesma, Teodoro S. Kaufman, Sebastián A. Testero, Enrique L. Larghi, Step-Economic Total Synthesis of Melosatin A from Eugenol, ACS Omega, 8, 25, (2023), 23174-23181 https://doi.org/10.1021/acsomega.3c02722
  8. Sally A. Hutchinson, Henning Luetjens, Peter J. Scammells, A new synthesis of the benzofuran adenosine antagonist XH-14, Bioorganic & Medicinal Chemistry Letters, 7, 24, (1997), 3081-3084 https://doi.org/10.1016/S0960-894X(97)10173-1
  9. Sabir H. Mashraqui, Chandrashekar D. Mudaliar, Harini Hariharasubrahmanian, 4,4-Dibromo-3-methylpyrazol-5-one: New applications for selective monobromination of phenols and oxidation of sulfides to sulfoxides, Tetrahedron Letters, 38, 27, (1997), 4865-4868 https://doi.org/10.1016/S0040-4039(97)01014-9
  10. Radia Mahboub, Faiza Memmou, Antioxidant activity and kinetics studies of eugenol and 6-bromoeugenol, Natural Product Research, 29, 10, (2015), 966-971 https://doi.org/10.1080/14786419.2014.958738
  11. Lisa I. Pilkington, David Barker, Synthesis of 3-Methylobovatol, Synlett, 26, 17, (2015), 2425-2428 https://doi.org/10.1055/s-0035-1560262
  12. Indranirekha Saikia, Arun Jyoti Borah, Prodeep Phukan, Use of Bromine and Bromo-Organic Compounds in Organic Synthesis, Chemical Reviews, 116, 12, (2016), 6837-7042 https://doi.org/10.1021/acs.chemrev.5b00400
  13. G. B. Frankforter, Max Lando, Eugenol and Some of Its Derivatives, Journal of the American Chemical Society, 27, 6, (1905), 641-649 https://doi.org/10.1021/ja01984a001
  14. Noël J. de Souza, A. N. Kothare, V. V. Nadkarny, Potential Antimicrobial Agents. Bromo Compounds of Eugenol, Journal of Medicinal Chemistry, 9, 4, (1966), 618-620 https://doi.org/10.1021/jm00322a045
  15. Kenneth M. Nicholas, Protecting group for the carbon-carbon double bond, Journal of the American Chemical Society, 97, 11, (1975), 3254-3255 https://doi.org/10.1021/ja00844a074
  16. Jean-Roger Desmurs, Isabelle Jouve, Alain Nonn, Procede de bromation de la double liaison de phenols ou de phenols substitues, a chaines ethyleniques, Paris AS 2631336, 1988
  17. Soad Mohamedeen Ahmed, Rasha El-Sayed Selim, Mohamed Salah Khalil, Saad Rashad El-Zemity, Monoterpenoids and Their Synthesized Brominate Derivatives as Eco-Friendly Measures to Control Some Plant Pathogenic Fungi and Bacteria, Asian Journal of Biological Sciences, 16, 3, (2023), 264-274 https://doi.org/10.3923/ajbs.2023.264.274
  18. Xiaojun Huang, Brandon Fulton, Kana White, Alejandro Bugarin, Metal-Free, Regio- and Stereoselective Synthesis of Linear (E)-Allylic Compounds Using C, N, O, and S Nucleophiles, Organic Letters, 17, 11, (2015), 2594-2597 https://doi.org/10.1021/acs.orglett.5b00862
  19. Selene Maia de Morais, Nadja Soares Vila-Nova, Claudia Maria Leal Bevilaqua, Fernanda Cristina Rondon, Carlos Henrique Lobo, Arlindo de Alencar Araripe Noronha Moura, Antônia Débora Sales, Ana Paula Ribeiro Rodrigues, José Ricardo de Figuereido, Claudio Cabral Campello, Mary E. Wilson, Heitor Franco de Andrade, Thymol and eugenol derivatives as potential antileishmanial agents, Bioorganic & Medicinal Chemistry, 22, 21, (2014), 6250-6255 https://doi.org/10.1016/j.bmc.2014.08.020
  20. Budi Arifin, Regioselektivitas Brominasi dengan Bromin Molekuler pada Eugenol dan Turunannya serta Aplikasi Turunan Bromo Eugenol untuk Sintesis Ester Koniferil, Institut Teknologi Bandung, Bandung, 2022
  21. John McMurry, Organic Chemistry, 10th ed., OpenStax, Texas, 2023,
  22. Taeko Irino, Kazuo Otsuki, Wagner-Meerwein Rearrangement of Allylbenzene Derivatives. I. Bromination of Safrole, Chemical and Pharmaceutical Bulletin, 23, 3, (1975), 646-650 https://doi.org/10.1248/cpb.23.646
  23. Olatunji S. Ojo, Alejandro Bugarin, One-Pot Synthesis of α-Alkyl Styrene Derivatives, ACS Omega, 6, 31, (2021), 20619-20628 https://doi.org/10.1021/acsomega.1c02801
  24. David Hardy, Stephen R. Isbel, Alejandro Bugarin, Durgesh V. Wagle, Quantum Chemical Insight into 1,2-Shift Rearrangement in Bromination of Allylaryls, ACS Omega, 8, 45, (2023), 42311-42318 https://doi.org/10.1021/acsomega.3c04513
  25. María E. Hidalgo, Carlos De la Rosa, Héctor Carrasco, Wilson Cardona, Claudio Gallardo, Luis Espinoza, Antioxidant capacity of eugenol derivatives, Quimica Nova, 32, 6, (2009), 1467-1470 https://doi.org/10.1590/S0100-40422009000600020
  26. Jaqueline Rosa Cardoso Barbosa, Murillo H. Queiroz, Roberto Rivelino, Gerlon de Almeida Ribeiro Oliveira, Luciano Morais Lião, Silvio Cunha, Regioselectivity in the Nitration of Eugenol Is Independent of Inorganic Reagents: An Experimental and Theoretical Investigation with Synthetic and Mechanistic Implications, The Journal of Organic Chemistry, 89, 2, (2023), 1120-1126 https://doi.org/10.1021/acs.joc.3c02298
  27. Eric V. Anslyn, Dennis A. Dougherty, Modern physical organic chemistry, University science books, 2006,

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