One-Pot Synthesis of 1-Benzoylpyrene over Heteropoly Acid Catalysts

2012 ◽  
Vol 560-561 ◽  
pp. 294-299
Author(s):  
Xiao Qing Lu ◽  
Min Xing ◽  
Ai Xia Pan ◽  
Yin Yin Wu ◽  
Ji Min Xie ◽  
...  

A novel one-pot catalytic synthesis of 1-benzoylpyrene through acylation of pyrene with benzoyl chloride catalyzed by various Keggin type heteropoly acids (salts) was investigated. Pure 1-benzoylpyrene was obtained and the structure of 1-benzoylpyrene was identified by GC/MS, FT-IR and 1H NMR spectra. H3PW12O40 (PW) was found to be the most active catalyst in the acylation. The yield and the selectivity of 1-benzoylpyrene were up to 97.6 % and 100 %, respectively. The effects of experimental parameters on the catalytic acylation reaction and the recycling performance of PW catalyst were studied. PW catalyst shows well catalytic activity after running for 5 times. The facile product separation and the recycling performance of PW catalyst is expected to contribute to the development of clean and environmentally friendly strategy for the synthesis of 1-benzoylpyrene.

2012 ◽  
Vol 560-561 ◽  
pp. 214-220
Author(s):  
Ai Xia Pan ◽  
Yin Yin Wu ◽  
Yu Fang ◽  
Lu Lu Xu ◽  
Min Chen

To obtain new fine chemical and intermediate of functional polymer material, the acylation of acenaphthene with benzoyl chloride to 5-acetylacenaphthene catalyzed by silica-supported phosphotungstic heteropoly acid (PW/SiO2) was investigated. Pure 5-acetylacenaphthene was obtained and its structure was identified by GC/MS, FT-IR and 1H NMR spectra. The effects of experimental parameters on the catalytic acylation reaction and the possibility of reusability of PW/SiO2 catalyst were studied. Under optimun conditions, the yield and the selectivity of 5-acetylacenaphthene were up to 81.3 % and 93.6 %, respectively. PW/SiO2 shows well catalytic activity after running for 5 times. The experimental results indicate that PW/SiO2 is a recyclable and environmentally benign catalyst in the synthesis of 5-acetylacenaphthene.


2011 ◽  
Vol 8 (2) ◽  
pp. 689-696 ◽  
Author(s):  
Fatemeh F. Bamoharram ◽  
Ali Ahmadpour ◽  
Majid M. Heravi ◽  
Mohammad J. Sane Charkhi

A rapid and efficient one-pot method for the synthesis ofβ-acetamido ketones/esters has been developed in the presence of bulk tungstophosphoric acid and its supported forms on activated carbon as recyclable and eco-friendly catalysts under refluxing conditions. Supported tungstophosphoric acid catalysts containing the same amount of heteropoly acid yielded much higher conversion than bulk form.


2006 ◽  
Vol 243 (2) ◽  
pp. 258-263 ◽  
Author(s):  
Enio José Leão Lana ◽  
Kelly A. da Silva Rocha ◽  
Ivan V. Kozhevnikov ◽  
Elena V. Gusevskaya

2012 ◽  
Vol 108 (2) ◽  
pp. 531-544 ◽  
Author(s):  
Min-Qiang He ◽  
Ai-Xia Pan ◽  
Ji-Min Xie ◽  
De-Li Jiang ◽  
Xin-Hua Yuan ◽  
...  

2011 ◽  
Vol 236-238 ◽  
pp. 1019-1022
Author(s):  
Bing Hu ◽  
Chuan Qun Hu ◽  
Long Hui Nie ◽  
Ming Xia Fan

The heteropoly acid catalyst of H5PMo10V2O40 supported on SBA-15 mesoporous mole-cular sieve was prepared by an impregnation method and characterized by nitrogen physisorption, FT-IR,SEM, and used in catalytic synthesis of tributyl citrate. The results show that the heteropoly acid catalyst has fine dispersion characteristics, structural stability, high catalytic activity and better reusability.


RSC Advances ◽  
2020 ◽  
Vol 10 (48) ◽  
pp. 28856-28864 ◽  
Author(s):  
Nikolay V. Gromov ◽  
Tatiana B. Medvedeva ◽  
Yulia A. Rodikova ◽  
Dmitrii E. Babushkin ◽  
Valentina N. Panchenko ◽  
...  

Influence of composition of catalysts based on heteropoly acid cesium salts on formic acid production via starch hydrolysis–oxidation was investigated.


2012 ◽  
Vol 443-444 ◽  
pp. 830-836
Author(s):  
Shu Yun Zhu ◽  
De Li Jiang ◽  
Yu Fang ◽  
Ji Min Xie ◽  
Min Chen

Acylation of acenaphthene with benzoyl chloride to 5-benzoylacenaphthene catalyzed by [Bmin]Cl/AlCl3 ([Bmin]+ = 1-butyl-3-methylimidazolium cation) ionic liquid was investigated. Pure 5-benzoylacenaphthene was obtained and the structure of 5-benzoylacenaphthene was identified by GC/MS, FT-IR and 1H NMR spectra. The yield of 5-benzoylacenaphthene was up to 85.2 % and the selectivity towards 5-benzoylacenaphthene was up to 89.6 %. The [Bmim]C1/A1C13 ionic liquid catalyst shows well catalytic activity after running for 5 times. The facile product separation and the recycling performance of the ionic liquid catalyst is expected to contribute to the development of clean and environmentally friendly strategy for the synthesis of 5-benzoylacenaphthene.


2010 ◽  
Vol 102 (1) ◽  
pp. 103-111 ◽  
Author(s):  
Min Chen ◽  
Yin-Yin Wu ◽  
Ying Luo ◽  
Min-Qiang He ◽  
Ji-Min Xie ◽  
...  

2020 ◽  
Vol 17 ◽  
Author(s):  
Saeid Azimi ◽  
Niloofar Mohamadighader

Abstract: A new solid catalyst was synthesized from an ionic liquid and heterogenised by changing anion reaction. The new heterogeneous acidic catalyst was characterized by SEM images, EDS analysis, AFM images, Ft-IR, HNMR, 13CNMR and Mass Spectroscopy. It was applied to synthesis of tri-arylmethanes throughout one-pot tri-component reactions among aromatic aldehydes, N,N-dimethylaniline and other carbonic nucleophiles such as anisole and indole. Hence, synthesis of convenient and inexpensive micro-heterogeneous catalyst was introduced, the efficiency of which was confirmed. Also, various useful products were synthesized throughout this simple and clean procedure.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mohammad Hossein Abdollahi-Basir ◽  
Boshra Mirhosseini-Eshkevari ◽  
Farzad Zamani ◽  
Mohammad Ali Ghasemzadeh

AbstractA one-pot three component reaction of benzaldehydes, 1H-tetrazole-5-amine, and 3-cyanoacetyl indole in the presence of a new hexamethylenetetramine-based ionic liquid/MIL-101(Cr) metal–organic framework as a recyclable catalyst was explored. This novel catalyst, which was fully characterized by XRD, FE-SEM, EDX, FT-IR, TGA, BET, and TEM exhibited outstanding catalytic activity for the preparation of a range of pharmaceutically important tetrazolo[1,5-a]pyrimidine-6-carbonitriles with good to excellent yields in short reaction time.


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