scholarly journals Chemicals from Biomass: Selective Synthesis of N-Substituted Furfuryl Amines by the One-Pot Direct Reductive Amination of Furanic Aldehydes

2019 ◽  
Vol 7 (6) ◽  
pp. 6243-6250 ◽  
Author(s):  
Andrea García-Ortiz ◽  
Juan D. Vidal ◽  
Maria J. Climent ◽  
Patricia Concepción ◽  
Avelino Corma ◽  
...  
Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 287
Author(s):  
Jianguo Liu ◽  
Mingyue Zhang ◽  
Longlong Ma

Dibenzylamine motifs are an important class of crucial organic compounds and are widely used in fine chemical and pharmaceutical industries. The development of the efficient, economical, and environmentally friendly synthesis of amines using transition metal-based heterogeneous catalysts remains both desirable and challenging. Herein, we prepared the covalent organic framework (COF)-supported heterogeneous reduced COF-supported Pd-based catalyst and used it for the one-pot reductive amination of aldehydes. There are both Pd metallic state and oxidated Pdσ+ in the catalysts. Furthermore, in the presence of the reduced COF-supported Pd-based catalyst, many aromatic, aliphatic, and heterocyclic aldehydes with various functional groups substituted were converted to their corresponding amines products in good to excellent selectivity (up to 91%) under mild reaction conditions (70 °C, 2 h, NH3, 20 bar H2). This work expands the covalent organic frameworks for the material family and its support catalyst, opening up new catalytic applications in the economical, practical, and effective synthesis of secondary amines.


2009 ◽  
Vol 11 (2) ◽  
pp. 265-268 ◽  
Author(s):  
Laura Rubio-Pérez ◽  
F. Javier Pérez-Flores ◽  
Pankaj Sharma ◽  
Luis Velasco ◽  
Armando Cabrera

2020 ◽  
Vol 7 (1) ◽  
pp. 82-90 ◽  
Author(s):  
Xiao Chen ◽  
Shuhua Han ◽  
Dongdong Yin ◽  
Changhai Liang

For the one-pot reductive amination of benzaldehyde with nitrobenzene, intermetallic Ni2Si/SiCN from the decomposition of a nickel-modified polysilazane precursor exhibited high activity (>99%) and high selectivity (92% to aromatic amine).


2020 ◽  
Vol 10 (13) ◽  
pp. 4201-4209
Author(s):  
Jin Hee Cho ◽  
Sangmoon Byun ◽  
Ahra Cho ◽  
B. Moon Kim

We have developed a new catalytic method for the one-pot, cascade synthesis of unsymmetrical secondary amines via the reductive amination of aryl nitriles with nitroalkanes using a PdPt–Fe3O4 nanoparticle (NP) catalyst.


ChemInform ◽  
2009 ◽  
Vol 40 (24) ◽  
Author(s):  
Laura Rubio-Perez ◽  
F. Javier Perez-Flores ◽  
Pankaj Sharma ◽  
Luis Velasco ◽  
Armando Cabrera

Molbank ◽  
10.3390/m1196 ◽  
2021 ◽  
Vol 2021 (1) ◽  
pp. M1196
Author(s):  
Diana Becerra ◽  
Hugo Rojas ◽  
Juan-Carlos Castillo

We reported an efficient one-pot two-step synthesis of 3-(tert-butyl)-N-(4-methoxybenzyl)-1-methyl-1H-pyrazol-5-amine 3 in good yield by a solvent-free condensation/reduction reaction sequence starting from 3-(tert-butyl)-1-methyl-1H-pyrazol-5-amine 1 and p-methoxybenzaldehyde 2. The one-pot reductive amination proceeded by the formation in situ of the N-(5-pyrazolyl)imine 4 as key synthetic intermediate of other valuable pyrazole derivatives. This methodology is distinguished by its operational easiness, short reaction time, isolation and purification of the aldimine intermediate is not required. The structure of the synthesized N-heterocyclic amine 3 was fully characterized by FTIR-ATR, 1D and 2D NMR experiments, EIMS, and elemental analysis.


CrystEngComm ◽  
2021 ◽  
Author(s):  
Lisa Allen ◽  
Josh Davies-Jones ◽  
Philip R. Rosser Davies ◽  
Sarah King ◽  
Padraic O’Reilly

The one-pot, shape selective synthesis of cerium phosphate nanorods has been explored and developed to give nanoparticles with aspect ratios between 3-24.8. Studies of the surface with Photo induced Force...


Molecules ◽  
2021 ◽  
Vol 26 (4) ◽  
pp. 1120
Author(s):  
Giuseppe Romanazzi ◽  
Valentina Petrelli ◽  
Ambra Maria Fiore ◽  
Piero Mastrorilli ◽  
Maria Michela Dell’Anna

Recently, N-substituted anilines have been the object of increasing research interest in the field of organic chemistry due to their role as key intermediates for the synthesis of important compounds such as polymers, dyes, drugs, agrochemicals and pharmaceutical products. Among the various methods reported in literature for the formation of C–N bonds to access secondary anilines, the one-pot reductive amination of aldehydes with nitroarenes is the most interesting procedure, because it allows to obtain diverse N-substituted aryl amines by simple reduction of nitro compounds followed by condensation with aldehydes and subsequent reduction of the imine intermediates. These kinds of tandem reactions are generally catalyzed by transition metal-based catalysts, mainly potentially reusable metal nanoparticles. The rapid growth in the last years in the field of metal-based heterogeneous catalysts for the one-pot reductive amination of aldehydes with nitroarenes demands for a review on the state of the art with a special emphasis on the different kinds of metals used as catalysts and their recyclability features.


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