Development of new supported catalysts for the continuous alkylation of amines with alcohols
https://doi.org/10.32362/2410-6593-2025-20-1-18-26
EDN: ILGHIV
Abstract
Objectives. The work set out to develop catalysts based on nickel and copper obtained by active phase chemical reduction and investigate their activity including the influence of the type of supports on the course of alkylation of amines with primary or secondary alcohols in a plug-flow reactor with a fixed catalyst bed.
Methods. The reactions were carried out in a continuous mode on a fixed bed of an appropriate catalyst in a plug flow microcatalytic apparatus at 160–240°C. NaX zeolite, magnesium oxide, and γ-Al2O3 were used as supports. After preparing the catalysts by impregnation from an excess solution of metal salts, the active metal phase was reduced with a sodium tetrahydridoborate aqueous solution. The composition of the resulting products was analyzed by gas–liquid chromatography, while their structure was confirmed by gas chromatography-mass spectrometry. The alkylating agents were ethanol, 2-propanol, 1-butanol, 1-pentanol, benzyl alcohol, and 1-octanol; alkylated amines were 1-butylamine, 1-hexylamine, 1-octylamine, aniline, morpholine, piperidine, and hexamethyleneimine.
Results. The alkylation of amines with alcohols catalyzed by metal (nickel and copper) nanoparticles supported on NaX zeolite, magnesium oxide MgO, and γ-Al2O3 in a plug-flow reactor with a fixed catalyst bed at atmospheric hydrogen pressure and 160–240°C leads to the formation of predominantly mono-N-alkylated products with yields up to 99%.
Conclusions. Nickel (or nickel and copper) nanoparticles supported on various supports are effective catalysts for the synthesis of secondary or tertiary amines in the plug-flow reactor.
About the Authors
V. M. MokhovRussian Federation
Vladimir M. Mokhov, Dr. Sci. (Chem.), Professor, Technology of Organic and Petrochemical Synthesis Department
Scopus Author ID 7003930850
28, pr. Imeni Lenina, Volgograd, 400005
Competing Interests:
The authors declare no conflicts of interest.
D. N. Nebykov
Russian Federation
Denis N. Nebykov, Cand. Sci. (Chem.), Associate Professor, Technology of Organic and Petrochemical Synthesis Department
Scopus Author ID 56146258500
28, pr. Imeni Lenina, Volgograd, 400005
Competing Interests:
The authors declare no conflicts of interest.
A. O. Panov
Russian Federation
Alexandr O. Panov, Senior Lecturer, Technology of Organic and Petrochemical Synthesis Department
Scopus Author ID 57193649148
28, pr. Imeni Lenina, Volgograd, 400005
Competing Interests:
The authors declare no conflicts of interest.
A. V. Razvalyaeva
Russian Federation
Anastasia V. Razvalyaeva, Assistant, Technology of Organic and Petrochemical Synthesis Department
Scopus Author ID 58205069200
28, pr. Imeni Lenina, Volgograd, 400005
Competing Interests:
The authors declare no conflicts of interest.
S. E. Latyshova
Russian Federation
Snezhana E. Latyshova, Cand. Sci. (Chem.), Associate Professor, Technology of Organic and Petrochemical Synthesis Department
Scopus Author ID 57193645336
28, pr. Imeni Lenina, Volgograd, 400005
Competing Interests:
The authors declare no conflicts of interest.
M. A. Vaniev
Russian Federation
Marat A. Vaniev, Dr. Sci. (Eng.), Heard of the Department of Chemistry and Technology of Elastomer Processing
Scopus Author ID 14063995400
28, pr. Imeni Lenina, Volgograd, 400005
Competing Interests:
The authors declare no conflicts of interest.
References
1. Hayes K.S. Industrial processes for manufacturing amines. Appl. Catal. A: Gen. 2001;221(1):187–195. https://doi.org/10.1016/S0926-860X(01)00813-4
2. Bayguzina A.R., Khusnutdinov R.I. Catalytic N-Alkylation of Anilines. Russ. J. Gen. Chem. 2021;91(3):305–347. https://doi.org/10.1134/S1070363221030014 [Original Russian Text: Bayguzina A.R., Khusnutdinov R.I. Catalytic N-Alkylation of Anilines. Zhurnal Obshchei Khimii. 2021;91(3):331–375 (in Russ.). https://doi.org/10.31857/S0044460X2103001X ]
3. Brown A.B., Reid E.E. Catalytic alkylation of aniline J. Am. Chem. Soc. 1924;46(8):1836–1839. https://doi.org/10.1021/ja01673a011
4. Chen A., Wang H., Liu R., Bo Y., Hu J. N-Alkylation of Alkylolamines with Alcohols Over Mesoporous Solid Acid–Base Cs–B–Zr Catalyst. Catal. Lett. 2016;146(7): 1182–1193. https://doi.org/10.1007/s10562-016-1737-2
5. Niu F., Wang Q., Yan Z., Kusema B.T., Khodakov A.Y., Ordomsky V.V. Highly Efficient and Selective N-Alkylation of Amines with Alcohols Catalyzed by in Situ Rehydrated Titanium Hydroxide. ACS Catal. 2020;10(5):3404−3414. https://doi.org/10.1021/acscatal.9b05525
6. Bayguzina А.R., Khusnutdinov R.I., Musina C.F. N-Alkylation of Aniline and Its Derivatives by Alcohols in the Presence of Copper Compounds. Russ. J. Org. Chem. 2018;54(11): 1652–1659. https://doi.org/10.1134/S1070428018110052 [Original Russian Text: Bayguzina А.R., Musina C.F., Khusnutdinov R.I. N-Alkylation of Aniline and Its Derivatives by Alcohols in the Presence of Copper Compounds. Zhurnal Organicheskoi Khimii. 2018;54(11):1642–1648 (in Russ.). https://doi.org/10.1134/S0514749218110055 ]
7. Yan T., Feringa B.L., Barta K. Iron catalysed direct alkylation of amines with alcohols. Nat. Commun. 2014;5:5602. https://doi.org/10.1038/ncomms6602
8. Ma Z., Zhou B., Li X., Kadam R.G., Gawande M.B., Petr M., Zboril R., Beller M., Jagadeesh R.V. Reusable Co-nanoparticles for general and selective N-alkylation of amines and ammonia with alcohols. Chem. Sci. 2022;13(1):111–117. https://doi.org/10.1039/d1sc05913k
9. Wang G., Sun L., Liu W., Zhan H., Bi S. Iron-nickel alloy particles with N-doped carbon “armor” as a highly selective and long-lasting catalyst for the synthesis of N-benzylaniline molecules. Nano Res. 2024;17(4):2308–2319. https://doi.org/10.1007/s12274-023-6041-z
10. Popov Yu.V., Mokhov V.M., Tankabekyan N.A. Colloid and nanodimensional catalysts in organic synthesis: III. Alkylation of amines with primary alcohols catalyzed by colloidal nickel and cobalt. Russ. J. Gen. Chem. 2014;84(5):826–830. https://doi.org/10.1134/S1070363214050065 [Original Russian Text: Popov Yu.V., Mokhov V.M., Tankabekyan N.A. Colloid and nanodimensional catalysts in organic synthesis: III. Alkylation of amines with primary alcohols catalyzed by colloidal nickel and cobalt. Zhurnal Obshchei Khimii. 2014;84(5):733–737 (in Russ.).]
11. Zou Y., Dong L., Yan S., Liu J., Mu L., Li L., Hu Y., Qi H., Mao S., Chen Z. Activity enhancement of Ru/CeO2 for N-alkylation of amines with alcohols through tailoring metalsupport interaction. J. Catalysis. 2024;429:115241. https://doi.org/10.1016/j.jcat.2023.115241
12. Zhang D., Tian J.., Yan Y., Zhang L., Hu H. Cu-decorating on N, P-Codoped porous carbon derived from wheat straw as advanced catalysts for N-alkylation of amines with alcohols. Arabian J. Chem. 2023;16(10):105124. https://doi.org/10.1016/j.arabjc.2023.105124
13. Pan J., Li J., Xia X.-F, Zeng W., Wang D. High Active Palladium Composite and Catalytic Applications on the Synthesis of Substituted Aminopyridine Derivatives Through Borrowing Hydrogen Strategy. Catal. Lett. 2023;153: 2378–2387. https://doi.org/10.1007/s10562-022-04024-0
14. Wu Y., Xi S., Chen C., Hu Q., Xiong Z., Wang J., Dai Y., Han Y., Jiang S., Wang J., Zhou Y. Synergistic roles of platinum nanoparticles and sodium ions within beta zeolites in N-alkylation of amines with aromatic alcohols. Sci. China Chem. 2023;66(9):2690–2699. https://doi.org/10.1007/s11426023-1719-y
15. Nebykov D.N., Panov A.O., Razvalyaeva A.V., Latyshova S.E., Mokhov V.M. Colloidal and Nanosized Catalysts in Organic Synthesis: XXVI. Amines Alkylation with Alcohols Catalyzed by γ-Al2O3-Supported Nickel and Copper Nanoparticles. Russ. J. Gen. Chem. 2023;93(8):1931–1940. https://doi.org/10.1134/S1070363223080017 [Original Russian Text: Nebykov D.N., Panov A.O., Razvalyaeva A.V., Latyshova S.E., Mokhov V.M. Colloidal and Nanosized Catalysts in Organic Synthesis: XXVI. Amines Alkylation with Alcohols Catalyzed by γ-Al2O3-Supported Nickel and Copper Nanoparticles. Zhurnal Obshchei Khimii. 2023;93(8):1151–1161 (in Russ.). https://doi.org/10.31857/S0044460X23080012 ]
16. Popov Yu.V., Mokhov V.M., Latyshova S.E., Nebykov D.N., Panov A.O., Davydova T.M. Colloid and Nanosized Catalysts in Organic Synthesis: XVIII. Disproportionation and CrossCoupling of Amines During Catalysis with Immobilized Nickel Nanoparticles. Russ. J. Gen. Chem. 2017;87(12): 2757–2761. https://doi.org/10.1134/S1070363217120015 [Original Russian Text: Popov Yu.V., Mokhov V.M., Latyshova S.E., Nebykov D.N., Panov A.O., Davydova T.M. Colloid and Nanosized Catalysts in Organic Synthesis: XVIII. Disproportionation and Cross-Coupling of Amines During Catalysis with Immobilized Nickel Nanoparticles. Zhurnal Obshchei Khimii. 2017;87(12):1937–1941 (in Russ.).]
17. Paputina A.N., Popov Yu.V., Mokhov V.M. Alkylation of amines by alkanols during catalysis by alloused nickel and copper nanoparticles. In: New Materials and Advanced Technologies: collection of materials of the Fifth Interdisciplinary Scientific Forum with International Participation. V. I. Moscow: Intellektual’nye sistemy; 2019. P. 218–219 (in Russ.).
18. Popov Yu.V., Mokhov V.M., Nebykov D.N., Paputina A.N., Nemtseva N.V. The secondary amines synthesis by alkylation of aniline with alcohols catalized by zeolite NaX supported nickel and copper nanoparticles. Izvestiya Volgogradskogo gosudarstvennogo tekhnicheskogo universiteta = Izvestia VSTU. 2019;12(235):60–63 (in Russ.).
- The alkylation of amines with alcohols catalyzed by metal (nickel and copper) nanoparticles supported on NaX zeolite, magnesium oxide MgO, and γ-Al2O3 in a plug-flow reactor with a fixed catalyst bed at atmospheric hydrogen pressure and 160–240°C leads to the formation of predominantly mono-N-alkylated products with yields up to 99%.
- Nickel (or nickel and copper) nanoparticles supported on various supports are effective catalysts for the synthesis of secondary or tertiary amines in the plug-flow reactor.
Review
For citations:
Mokhov V.M., Nebykov D.N., Panov A.O., Razvalyaeva A.V., Latyshova S.E., Vaniev M.A. Development of new supported catalysts for the continuous alkylation of amines with alcohols. Fine Chemical Technologies. 2025;20(1):18-26. https://doi.org/10.32362/2410-6593-2025-20-1-18-26. EDN: ILGHIV