scholarly journals Graphene encapsulated low-load nitrogen-doped bimetallic magnetic Pd/Fe@N/C catalyst for the reductive amination of nitroarene under mild conditions

Author(s):  
Jianguo liu ◽  
Shanshan Lin ◽  
Longlong Ma

Aniline is a group of important platform molecules and is widely used in the synthesis of other high-value chemicals and pharmaceutical products. How to produce high-value anilines as the high-value chemical intermediates more efficiently and more environmentally has always been a research topic in the industry. Catalytic hydrogenation is an environmentally friendly method for preparing halogenated anilines. Traditional noble metals catalysis face cost and noble metals residue problems. To improve the purity of the product and the activity and recyclability of the catalyst, we prepared a Pd/Fe magnetic bimetallic catalyst supported on N-doped carbon materials to reduce nitrobenzene to aniline under mild conditions. The loading of Pd was very low, which was 1/10 of the content of common commercial precious metal Pd/C and Pt/C catalysts, which was only 0.5%. And the prepared bimetallic Pd/Fe@N/C catalyst showed excellent catalytic reactivity with the conversion rate of nitrobenzene > 99%, and the selectivity of aniline 99% under mild reaction conditions of 0.8 MPa H2 and 40 °C. A variety of halogenated and aliphatic nitro compounds were well tolerated and had been transformed to the corresponding target amine products with excellent selectivity. In addition, the novel N-doped graphene-encapsulated bimetallic magnetic Pd/Fe@N/C catalyst not only had magnetic physical properties, which was easy to separate, recover, and used for the recycling of the catalyst without metal leaching but also catalyzed highly selective reductive amination of aromatics was a green, economical and environmentally friendly reaction with the only H2O as a by-product.

2021 ◽  
Vol 18 ◽  
Author(s):  
Adilakshmi Singavarapu ◽  
Gowri Sankar Reddipalli ◽  
Venkat Reddy Ghojala

: The novel synthetic route to an antipsychotic drug Cariprazine was developed and demonstrated on a commercial scale. The synthesis of Cariprazine is achieved from N-(4-oxocyclohexyl) acetamide by using various reactions such as Wittig-Horner reaction, reduction of alkene, hydrolysis of ester, deacylation, amidation, reduction of weinreb amide to yield the corresponding aldehyde, and finally reductive amination of aldehyde in presence of the corresponding amine to form Cariprazine. In this article, we report a novel intermediate 2-[trans-4-(3,3-Dimethylureido)cyclohexyl]-N-methoxy-N-methylacetamide by avoiding potentially genotoxic substances/intermediates, tedious, drastic reaction conditions.


Synlett ◽  
2020 ◽  
Author(s):  
Yong-Zhou Pan ◽  
Shi-Yan Cheng ◽  
Qian-Yu Li ◽  
Hai-Tao Tang ◽  
Ying-Ming Pan ◽  
...  

The novel method for the synthesis of gem-bisarylthio enamines and α-phenylthio ketones was developed via the coupling of α-substituted vinyl azides with thiols in the presence of tetrabutylammonium iodide (TBAI) as a redox catalyst and electrolyte at room temperature. Electronic properties were crucial in the generated products. This protocol features metal- and oxidant-free materials, broad tolerance of substrates, and mild reaction conditions.


2021 ◽  
Author(s):  
Baixue Li ◽  
Jia Wang ◽  
Anjun Qin ◽  
Ben Zhong Tang

An efficient imidazole-based Cu(i)-catalyzed azide–alkyne click polymerization under mild reaction conditions was developed.


Author(s):  
Evelyn Alves Nunes Simonetti ◽  
Thais Cardoso de Oliveira ◽  
Ádamo Enrico do Carmo Machado ◽  
Amanda Alvarenga Coutinho Silva ◽  
Alan Silva dos Santos ◽  
...  

2021 ◽  
Author(s):  
Seyyedeh Ameneh Alavi G. ◽  
Mohammad Ali Nasseri ◽  
Milad Kazemnejadi ◽  
Ali Allahresani ◽  
Mahdi HussainZadeh

The novel heterogeneous bimetallic nanoparticles of Cu–Co were synthesized and successfully applied as a recyclable magnetically catalyst in Heck, Suzuki, and C–N cross-coupling via a quick, easy, efficacious and environmentally protocol.


2021 ◽  
Vol 505 ◽  
pp. 111504
Author(s):  
Lin Liu ◽  
Wenxiu Li ◽  
Ran Qi ◽  
Qingqing Zhu ◽  
Jing Li ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1466
Author(s):  
Ye Eun Kim ◽  
Hyunsung Cho ◽  
Yoo Jin Lim ◽  
Chorong Kim ◽  
Sang Hyup Lee

Studies on a one-pot synthesis of novel multisubstituted 1-alkoxyindoles 1 and their mechanistic investigations are presented. The synthesis of 1 was successfully achieved through consecutive four step reactions from substrates 2. The substrates 2, prepared through a two-step synthetic sequence, underwent three consecutive reactions of nitro reduction, intramolecular condensation, and nucleophilic 1,5-addition to provide the intermediates, 1-hydroxyindoles 8, which then were alkylated in situ with alkyl halide to afford the novel target products 1. We optimized the reaction conditions for 1 focusing on the alkylation step, along with the consideration of formation of intermediates 8. The optimized condition was SnCl2·2H2O (3.3 eq) and alcohols (R1OH, 2.0 eq) for 1–2 h at 40 °C and then, base (10 eq) and alkyl halides (R2Y, 2.0 eq) for 1–4 h at 25–50 °C. Notably, all four step reactions were performed in one-pot to give 1 in good to modest yields. Furthermore, the mechanistic aspects were also discussed regarding the reaction pathways and the formation of side products. The significance lies in development of efficient one-pot reactions and in generation of new 1-alkoxyindoles.


2021 ◽  
pp. 174751982110325
Author(s):  
Yan Xiao ◽  
Jiyu Gao ◽  
Peng Chen ◽  
Guangliang Chen ◽  
Zicheng Li ◽  
...  

A series of symmetrical 1,4-disubstituted buta-1,3-diynes is prepared with excellent yields (up to 95%) through homocoupling of terminal alkynes catalyzed by a copper salt under solvent-free conditions. This method provides an environmentally friendly process to prepare 1,3-diynes in short reaction times under mild conditions. Furthermore, the method is suitable for a wide substrate scope and has excellent functional group compatibility. The reaction can also be scaled up to gram level.


Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5270
Author(s):  
Zhenbo Yuan ◽  
Xuanzhong Liu ◽  
Changmei Liu ◽  
Yan Zhang ◽  
Yijian Rao

Non-proteinogenic amino acids have attracted tremendous interest for their essential applications in the realm of biology and chemistry. Recently, rising C–H functionalization has been considered an alternative powerful method for the direct synthesis of non-proteinogenic amino acids. Meanwhile, photochemistry has become popular for its predominant advantages of mild conditions and conservation of energy. Therefore, C–H functionalization and photochemistry have been merged to synthesize diverse non-proteinogenic amino acids in a mild and environmentally friendly way. In this review, the recent developments in the photo-mediated C–H functionalization of proteinogenic amino acids derivatives for the rapid synthesis of versatile non-proteinogenic amino acids are presented. Moreover, postulated mechanisms are also described wherever needed.


2020 ◽  
Vol 9 (1) ◽  
pp. 139-152 ◽  
Author(s):  
Xiao Zhang ◽  
Yanlu Liu ◽  
Panfang Lu ◽  
Min Zhang

AbstractA novel hydrogel slow-release nitrogen fertilizer based on sawdust with water absorbency was prepared using grafting copolymerization. Urea was incorporated as nitrogen source in a hydrogel fertilizer. Potassium persulfate (KPS) and N,N᾽-methylenebis acrylamide (MBA) were used as the initiator and cross-linker, respectively. The structure and properties of the samples were characterized by XPS, EDS, SEM, XRD and FTIR. The effects of various salt solutions, ionic strength and pH on swelling behavior were discussed. The results showed that the largest water absorbency of the sample reached 210 g/g in distilled water. In addition, the sample had the good nitrogen release property. Thus, the novel environmentally friendly hydrogel fertilizer may be widely applied to agricultural and horticultural fields.


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