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Minqiang He,Min Chen,Aixia Pan,Jimin Xie,Huamin Li,Xinhua Yuan,Xiaonong Cheng 한국화학공학회 2012 Korean Journal of Chemical Engineering Vol.29 No.10
A novel one-pot catalytic synthesis of 1-benzoylpyrene through acylation of pyrene with benzoic anhydride catalyzed by several heteropoly acids (HPAs) was investigated. Pure 1-benzoylpyrene was obtained and its structure was identified by GC/MS, FT-IR and 1H NMR spectra. Silica-supported phosphotungstic heteropoly acid (PW/SiO2)was found to be the most active catalyst in the acylation. The yield and the selectivity of 1-benzoylpyrene were up to 62.5% and 100%, respectively. The effects of experimental parameters on the catalytic acylation reaction, and the possibility of reusability of PW/SiO2 catalyst were studied. PW/SiO2 catalyst is easily separable from the reaction mixture and reusable without loss of its activity.
Alkylation of anthracene to 2-isopropylanthracene catalyzed by Lewis acid ionic liquids
Min Chen,Ying Luo,Guofang Li,Minqiang He,Jimin Xie,Huamin Li,Xinhua Yuan 한국화학공학회 2009 Korean Journal of Chemical Engineering Vol.26 No.6
Alkylation of anthracene with 2-chloropropane to 2-isopropylanthracene catalyzed by various Lewis acidic ionic liquids (ILs), such as [Emim]Cl-AlCl3, [Emim]Cl-FeCl3, [Emim]Cl-ZnCl2, [Bmim]Cl-AlCl3, and [Omim]Cl-AlCl3 ([Emim]+=1-ethyl-3-methylimidazolium cation, [Bmim]+=1-butyl-3-methylimidazolium cation, [Omim]+=1-octyl-3- methylimidazolium cation,), was investigated. [Emim]C1-A1C13 ionic liquid was found to be the most active catalyst in the alkylation. The yield of 2-isopropylanthracene was up to 74.5% and the selectivity of 2-isopropylanthracene was up to 82.9%. The [Emim]C1-A1C13 ionic liquid catalyst showed good catalytic activity after running for 6 times. Ease of 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 2-isopropylanthracene.
Synthesis of 5-benzoylacenaphthene in the presence of Lewis acidic ionic liquids
Min Chen,Di Li,Ying Luo,Minqiang He,Jimin Xie,Huamin Li,Xinhua Yuan 한국공업화학회 2011 Journal of Industrial and Engineering Chemistry Vol.17 No.1
Acylation of acenaphthene with benzoyl chloride to 5-benzoylacenaphthene catalyzed by various Lewis acidic ionic liquids (ILs) was investigated. Ionic liquids of different alkyl chain length and metal chloride were synthesized and tested for the reaction to discuss the effects of Lewis acidity of the ionic liquid on the synthesis of 5-benzoylacenaphthene. Pure 5-benzoylacenaphthene was obtained and its structure was identified by GC/MS, FT-IR and 1H NMR spectra. [Emim]Cl/AlCl3 ionic liquid was found to be the most active catalyst in the acylation. The yield of 5-benzoylacenaphthene was up to 87% and the regioselectivity towards 5-benzoylacenaphthene was up to 90%. The experimental resulted show that [Emim]Cl/AlCl3 can be used as both catalyst and solvent, and it is reusable and environmentally friendly for the preparation of 5-benzoylacenaphthene.