Application of carbonate solvents in the telomerisation of butadiene with carbon dioxide

被引:54
作者
Behr, Arno [1 ]
Bahke, Philip [1 ]
Klinger, Ben [1 ]
Becker, Marc [1 ]
机构
[1] Univ Dortmund, Lehrstuhl Tech Chem A, D-44227 Dortmund, Germany
关键词
telomerisation; carbon-dioxide activation; butadiene; carbonate solvents; Pd-catalysis;
D O I
10.1016/j.molcata.2006.11.043
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This contribution describes the synthesis of the delta-lactone 2-ethylidene-6-heptene-5-olide from the reactants 1,3-butadiene and carbon dioxide in carbonate solvents. Palladiumbis(acetyl acetonate) in combination with the ligand triphenylphosphine is used as homogeneous catalyst. At a reaction temperature of 60-100 degrees C yields of the delta-lactone up to 50% can be achieved in a reaction time of 4 h. The use of green solvents like carbonates in this reaction is new, as mainly toxic nitrile solvents such as acetonitrile are known from literature till now. In this work we examined in detail the application and the influence on the selectivity of linear carbonates (dimethyl and diethyl carbonate), cyclic carbonates (ethylene carbonate, propylene carbonate and butylene carbonate) and glycerol carbonate esters in the telomerisation of butadiene with carbon dioxide. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 156
页数:8
相关论文
共 17 条
[1]  
BAHKE P, 2005, THESIS U DORTMUND
[2]  
Behr A, 2000, CHEM ENG TECHNOL, V23, P952, DOI 10.1002/1521-4125(200011)23:11<952::AID-CEAT952>3.0.CO
[3]  
2-0
[4]   Homogeneous and heterogeneous catalyzed three-step synthesis of 2-ethylheptanoic acid from carbon dioxide, butadiene and hydrogen [J].
Behr, A ;
Brehme, VA .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2002, 187 (01) :69-80
[5]  
Behr A, 2002, ADV SYNTH CATAL, V344, P525, DOI 10.1002/1615-4169(200207)344:5<525::AID-ADSC525>3.0.CO
[6]  
2-U
[7]   POSSIBILITIES OF CONTROLLING TRANSITION METAL-CATALYZED REACTIONS OF 1,3-DIENES WITH CARBON-DIOXIDE [J].
BEHR, A ;
HE, R ;
JUSZAK, KD ;
KRUGER, C ;
TSAY, YH .
CHEMISCHE BERICHTE-RECUEIL, 1986, 119 (03) :991-1015
[8]  
Behr A., 1988, CARBON DIOXIDE ACTIV
[9]  
Behr A., 2004, CHEM-ING-TECH, V76, P1828, DOI DOI 10.1002/CITE.200400087
[10]  
BEHR A, 2003, ANN M GERM CAT SOC W