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DOI: 10.1055/s-0043-1777286
Kinetic Study of the Acylation Reaction of Dibutylcarbamyl Chloride and Dibutylamine
Funding We are grateful to the Zhejiang Provincial Key R&D Project (Grant. No. 2020C03006 & 2019-ZJ-JS-03) for financial support.Abstract
Tetrabutylurea (TBU) is mainly used as a working liquid in the preparation of hydrogen peroxide via the anthraquinone process. It is reported that dibutylamine (A) reacts with dibutylcarbamyl chloride (B) to produce TBU in the presence of triphosgene, which is the decisive step of the reaction. In this study, we aimed to investigate the reaction kinetics of the decisive step to gain more insight into the reaction. The reaction order as well as the pre-exponential factors (A) and the activation energies (E a) were determined. The kinetic study suggested that the total order of the reaction is second. E a = 5.4 × 104 J/mol, A = 1.5257 × 107 L/(mol × min), calculated through a second-order kinetics model. The accuracy and applicability of the kinetic model were verified by serval experiments, showing that enhancing reaction temperature could shorten the reaction time and increase the conversion rate.
Publikationsverlauf
Eingereicht: 30. Juli 2023
Angenommen: 01. November 2023
Artikel online veröffentlicht:
04. Dezember 2023
© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)
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References
- 1 Ghosh AK, Kovela S, Osswald HL. et al. Structure-based design of highly potent HIV-1 protease inhibitors containing new tricyclic ring P2-ligands: design, synthesis, biological, and X-ray structural studies. J Med Chem 2020; 63 (09) 4867-4879
- 2 Garuti L, Roberti M, Bottegoni G, Ferraro M. Diaryl urea: a privileged structure in anticancer agents. Curr Med Chem 2016; 23 (15) 1528-1548
- 3 Ronchetti R, Moroni G, Carotti A, Gioiello A, Camaioni E. Recent advances in urea- and thiourea-containing compounds: focus on innovative approaches in medicinal chemistry and organic synthesis. RSC Med Chem 2021; 12 (07) 1046-1064
- 4 Siddiqui N, Alam MS, Stables JP. Synthesis and anticonvulsant properties of 1-(amino-N-arylmethanethio)-3-(1-substituted benzyl-2, 3-dioxoindolin-5-yl) urea derivatives. Eur J Med Chem 2011; 46 (06) 2236-2242
- 5 Ertl P, Altmann E, McKenna JM. The most common functional groups in bioactive molecules and how their popularity has evolved over time. J Med Chem 2020; 63 (15) 8408-8418
- 6 Li HQ, Lv PC, Yan T, Zhu HL. Urea derivatives as anticancer agents. Anticancer Agents Med Chem 2009; 9 (04) 471-480
- 7 Batra S, Tusi Z, Madapa S. Medicinal chemistry of ureido derivatives as anti-infectives. Anti-Cancer Agent Me 2006; 5 (02) 135-160
- 8 Hodge CN, Aldrich PE, Bacheler LT. et al. Improved cyclic urea inhibitors of the HIV-1 protease: synthesis, potency, resistance profile, human pharmacokinetics and X-ray crystal structure of DMP 450. Chem Biol 1996; 3 (04) 301-314
- 9 Wilhelm S, Carter C, Lynch M. et al. Discovery and development of sorafenib: a multikinase inhibitor for treating cancer. Nat Rev Drug Discov 2006; 5 (10) 835-844
- 10 Borsini F, Evans K, Jason K, Rohde F, Alexander B, Pollentier S. Pharmacology of flibanserin. CNS Drug Rev 2002; 8 (02) 117-142
- 11 Agai-Csongor E, Domány G, Nógrádi K. et al. Discovery of cariprazine (RGH-188): a novel antipsychotic acting on dopamine D3/D2 receptors. Bioorg Med Chem Lett 2012; 22 (10) 3437-3440
- 12 Lemoucheux L, Rouden J, Ibazizene M, Sobrio F, Lasne MC. Debenzylation of tertiary amines using phosgene or triphosgene: an efficient and rapid procedure for the preparation of carbamoyl chlorides and unsymmetrical ureas. Application in carbon-11 chemistry. J Org Chem 2003; 68 (19) 7289-7297
- 13 Bana P, Lakó A, Kiss NZ. Synthesis of urea derivatives in two sequential continuous-flow reactors. Org Process Res Dev 2017; 21 (04) 611-622
- 14 Liu P, Wang Z, Hu X. Highly efficient synthesis of ureas and carbamates from amides by iodosylbenzene-induced hofmann rearrangement. Eur J Org Chem 2012; 10: 1994-2000
- 15 Liang J, Cochran JE, Dorsch WA. et al. Development of a scalable synthesis of an azaindolyl-pyrimidine inhibitor of influenza virus replication. Org Process Res Dev 2016; 20 (05) 965-969
- 16 Narendra N, Chennakrishnareddy G, Sureshbabu VV. Application of carbodiimide mediated Lossen rearrangement for the synthesis of alpha-ureidopeptides and peptidyl ureas employing N-urethane alpha-amino/peptidyl hydroxamic acids. Org Biomol Chem 2009; 7 (17) 3520-3526
- 17 Wang CH, Hsieh TH, Lin CC. et al. One-Pot synthesis of N-monosubstituted ureas from nitriles via tiemann rearrangement. Synlett 2015; 26 (13) 1823-1826
- 18 Nishizawa A, Takahira T, Yasui K. et al. Nickel-catalyzed decarboxylation of aryl carbamates for converting phenols into aromatic amines. J Am Chem Soc 2019; 141 (18) 7261-7265
- 19 Singh DV, Adeppa K, Misra K. Mechanism of isoproturon resistance in Phalaris minor: in silico design, synthesis and testing of some novel herbicides for regaining sensitivity. J Mol Model 2012; 18 (04) 1431-1445
- 20 Wu CY, Cheng HY, Liu RX. et al. Synthesis of urea derivatives from amines and CO2 in the absence of catalyst and solvent. Green Chem 2010; 12: 1811-1816
- 21 Ma HQ, Shen C, Feng B. et al. Research progress in synthesis of tetrabutylurea and its application in production of hydrogen peroxide. Chem Propell Polym Mater 2021; 19 (04) 26-31
- 22 Ma HQ, Ma YH, Zhao XD. et al. The invention relates to a method for preparing tetrabutylurea by aqueous phase method. CN Patent 108329238B. October, 2020