Esterification of Acetic Acid with n-Butanol Catalyzed by Metallocenes

被引:0
作者
Xu Sheng [1 ]
Li Hongbin [2 ]
Lin Qiuning [1 ]
Zeng Fanhua [1 ]
Shen Jie [1 ]
Yan Xiuwei [1 ]
Mi Puke [1 ]
机构
[1] E China Univ Sci & Technol, Dept Chem, Sch Chem & mol Engn, Shanghai 200237, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
关键词
metallocene; supported catalyst; acetic acid; n-butanol; esterification; TITANOCENE; TRANSESTERIFICATION; COMPLEXES; ZIRCONIA; SYSTEM;
D O I
暂无
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Efficient esterification of acetic acid with n-butanol has been achieved using metallocenes as the catalyst, and the ester can be produced with a high yield. The effect of several factors such as reaction time, molar ratio of catalyst/alcohol, and different metallocenes on the yield has been investigated. The results of homogeneous catalytic reaction show that Cp2Fe, Cp2TiCl2, Cp2ZrCl2, and [o-MeOC6H4C(Et)(2)Cp](2)ZrCl2 are effective catalysts for aliphatic acid esterification at a very low catalyst/alcohol molar ratio. When Cp2TiCl2 was used as the catalyst at a molar ratio of Ti/n-butanol equal to 0.049%, 90% yield was gained after 30 min. Silica gel (400 mesh) was used as the support to load metallocenes. The supported Cp2ZrCl2 catalyst exhibits high activity as that of Cp2ZrCl2 under optimum experimental conditions (calcination temperature = 400 degrees C, calcination time = 4.0 h, the molar ratio of Zr/butanol = 0.487%, reaction time = 45 min) with the ester yield of 90.6%. The use of supported metallocenes as the catalysts results in a cleaner process for esterification without wastewater produced. Moreover, the catalyst is easy to recycle.
引用
收藏
页码:365 / 369
页数:5
相关论文
共 23 条
[1]   Aryl-aryl bond formation by transition-metal-catalyzed direct arylation [J].
Alberico, Dino ;
Scott, Mark E. ;
Lautens, Mark .
CHEMICAL REVIEWS, 2007, 107 (01) :174-238
[2]   Dehydrogenative coupling of hydrostannanes catalyzed by transition-metal complexes [J].
Braunstein, P ;
Morise, X .
CHEMICAL REVIEWS, 2000, 100 (10) :3541-3552
[3]   Chemical redox agents for organometallic chemistry [J].
Connelly, NG ;
Geiger, WE .
CHEMICAL REVIEWS, 1996, 96 (02) :877-910
[4]   Asymmetric catalysis with chiral ferrocene ligands [J].
Dai, LX ;
Tu, T ;
You, SL ;
Deng, WP ;
Hou, XL .
ACCOUNTS OF CHEMICAL RESEARCH, 2003, 36 (09) :659-667
[5]   Common relationships of ferrocene oxidation with oxygen and sulfur dioxide in acid solutions and of its direct oxidation with carboxylic acids [J].
Fomin, V. M. .
RUSSIAN JOURNAL OF GENERAL CHEMISTRY, 2007, 77 (05) :954-960
[6]   Transesterfication of soybean oil catalyzed by sulfated ziconia [J].
Garcia, Camila Martins ;
Teixeira, Sergio ;
Marciniuk, Leticia Ledo ;
Schuchardt, Ulf .
BIORESOURCE TECHNOLOGY, 2008, 99 (14) :6608-6613
[7]   Solid acid catalysis using ion-exchange resins [J].
Harmer, MA ;
Sun, Q .
APPLIED CATALYSIS A-GENERAL, 2001, 221 (1-2) :45-62
[8]  
Huang JL, 2005, CHINESE J CATAL, V26, P203
[9]   Preparation and catalytic application of novel water tolerant solid acid catalysts of zirconium sulfate/HZSM-5 [J].
Jiang Ya-jie ;
Juan, Joon Ching ;
Meng Xiu-juan ;
Cao Wei-liang ;
Yarmo, Mohd Ambar ;
Zhang Jing-chang .
CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 2007, 23 (03) :349-354
[10]  
Kim HJ, 2004, STUD SURF SCI CATAL, V153, P201