scholarly journals H3PW12O40: An Efficient and Recyclable Heterogeneous Catalyst for the Selective Synthesis of 2-Aryl-5,6-dihydro-4H-1,3-oxazines and 2-Aryl-1,4,5,6-tetrahydropyrimidines

2010 ◽  
Vol 65 (4) ◽  
pp. 461-469 ◽  
Author(s):  
Iraj Mohammadpoor-Baltork ◽  
Majid Moghadam ◽  
Shahram Tangestaninejad ◽  
Valiollah Mirkhani ◽  
Zohre Eskandari

An environmentally friendly and highly efficient procedure has been developed for the selective synthesis of 2-aryl-5,6-dihydro-4H-1,3-oxazines and 2-aryl-1,4,5,6-tetrahydropyrimidines by cyclocondensation of arylnitriles with 3-amino-1-propanol and 1,3-diaminopropane in the presence of catalytic amounts of H3PW12O40 under thermal conditions and MW irradiation. Under the same reaction conditions, dicyanobenzenes are transformed to their corresponding mono-oxazines and monotetrahydropyrimidines with excellent chemoselectivity. These reactions are simple and clean, giving the products in high yields and high purity. The catalyst can be easily recovered after the reaction and reused efficiently in subsequent runs.

Author(s):  
Udayakumar Veerabagu ◽  
Gowsika Jaikumar ◽  
Fushen Lu ◽  
Franck Quero

The 3 wt% CuI/BNNS catalyst exhibited high efficiency for C–H difluoromethylation reactions and enabled greener synthesis at high yields using cyrene as a solvent. Furthermore, the catalyst could be easily recovered and recycled for at least five cycles.


2018 ◽  
Vol 73 (9) ◽  
pp. 641-645 ◽  
Author(s):  
Sepehr Sadegh-Samiei ◽  
Shahrzad Abdolmohammadi

AbstractA novel and efficient synthesis of eight 5-aryl-1,3-dimethyl-2,4-dioxo-1,2,3,4,5,8-hexahydropyrido[2,3-d]pyrimidine-7-carboxylic acids using a TiO2/SiO2 nanocomposite with a molar ratio of 1:1 as a recyclable heterogeneous catalyst is described. The desired products, five of which are new, are formed in short reaction times (2–3 h) with high to excellent yields (94%–98%) under very moderate reaction conditions (room temperature, aqueous media).


2020 ◽  
Vol 18 (6) ◽  
pp. 1155-1164 ◽  
Author(s):  
Sachin Choudhary ◽  
Jyothi Yadav ◽  
Mamta ◽  
Amol Prakash Pawar ◽  
Satheeshvarma Vanaparthi ◽  
...  

A simple and straightforward method for the synthesis of 4-iodo and 5-iodopyrrole-3-carboxaldehydes is developed in good to high yields (up to 78%) from a common set of starting materials by tuning the reaction conditions.


2020 ◽  
Vol 44 (9-10) ◽  
pp. 592-597
Author(s):  
Lin Jiang ◽  
Wen-Fei Jin ◽  
Liu-Dong Yu ◽  
Ming-Wei Yuan ◽  
Hong-Li Li ◽  
...  

A straightforward synthesis of benzonitriles is achieved via amino-catalyzed [3+3] benzannulation of α,β-unsaturated aldehydes and 4-arylsulfonyl-2-butenenitriles. Using pyrrolidine as an organocatalyst via iminium activation, a series of substituted benzonitriles were obtained in good to high yields in a regioselective manner. This reaction can proceed smoothly under mild reaction conditions and without the aid of any metals, additional oxidants, or strong bases, thus making this an efficient and environmentally friendly method to access benzonitriles.


2015 ◽  
Vol 39 (10) ◽  
pp. 7988-7997 ◽  
Author(s):  
Barahman Movassagh ◽  
Nasrin Rezaei

We have prepared a highly active and recyclable heterogeneous catalyst for the Heck reaction in aqueous media in high yields.


2013 ◽  
Vol 2013 ◽  
pp. 1-4
Author(s):  
Liangliang Han ◽  
Tao Wu ◽  
Zhongqiang Zhou

A simple and efficient procedure for the synthesis of 5-arylidenerhodanines by condensation of aromatic aldehydes with rhodanine in water using diammonium hydrogen phosphate as catalyst is described. The procedure offers several advantages including environmentally friendly, mild reaction conditions, short reaction times, high yields, and simple experimental and work-up procedures.


RSC Advances ◽  
2015 ◽  
Vol 5 (20) ◽  
pp. 15274-15282 ◽  
Author(s):  
Forouz Rastegari ◽  
Iraj Mohammadpoor-Baltork ◽  
Ahmad R. Khosropour ◽  
Shahram Tangestaninejad ◽  
Valiollah Mirkhani ◽  
...  

An efficient procedure for the synthesis of isobenzofuran-1(3H)-one derivatives in the presence of [HSO3PMIM]OTf–SiO2@MNPs as a highly recyclable catalyst under solvent-free thermal conditions and MW irradiation is reported.


2021 ◽  
Vol 99 (1) ◽  
pp. 72-78
Author(s):  
Shiva Zafari ◽  
Ramin Ghorbani-Vaghei ◽  
Sedigheh Alavinia

In this study, a novel heterogeneous catalyst (H3PW12O40/Fe3O4@SiO2-Pr-Pi) was prepared via immobilization of H3PW12O40 on the surface of piperidine modified magnetic nanoparticles (Fe3O4@SiO2-Pr-Pi). The synthesis of dihydro-2-oxypyrrole derivatives was carried out by the reaction of substituted aniline, formaldehyde, and dimethyl acetylenedicarboxylate, promoted by H3PW12O40/Fe3O4@SiO2-Pr-Pi in EtOH. The formation of resultant catalyst was confirmed by FTIR spectroscopy, FE-SEM, EDX, VSM, and TGA techniques. The magnetically separable and environmentally friendly nanostructured catalyst remained quite stable during reaction conditions and was reused for at least five recycle runs.


ChemInform ◽  
2010 ◽  
Vol 41 (36) ◽  
pp. no-no
Author(s):  
Iraj Mohammadpoor-Baltork ◽  
Majid Moghadam ◽  
Shahram Tangestaninejad ◽  
Valiollah Mirkhani ◽  
Zohre Eskandari

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