Ultrasound-Induced CO2/H2O Emulsions as a Medium for Clean Product Formation and Separation: The Barbier Reaction as a Synthetic Example

被引:9
作者
Cenci, Steven M. [1 ]
Cox, Liam R. [2 ]
Leeke, Gary A. [1 ]
机构
[1] Univ Birmingham, Sch Chem Engn, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
Carbon dioxide; Mixing; Emulsion; Mass transfer; Allylation; Aqueous media; Biphasic; Sonication; Kinetics; SUPERCRITICAL CARBON-DIOXIDE; SOLUBLE METAL-COMPLEXES; AQUEOUS-MEDIA; PARTITION-COEFFICIENTS; HOMOALLYLIC ALCOHOLS; EFFICIENT SYNTHESIS; ORGANIC-SYNTHESIS; IONIC LIQUIDS; WATER; ALLYLATION;
D O I
10.1021/sc500112q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Subcritical CO2/H2O (30 degrees C/80 bar) was employed as a renewable solvent mixture in a 1 dm(3) ultrasound reactor. As a representative synthetic transformation, the metal-mediated Barbier allylation was used to demonstrate the facility of formation and separation of the homoallylic alcohol product. The chemoselectivity over the competing aldehyde reduction could be improved by deploying the biocompatible nonionic surfactant Tween 80, a saturated salt aqueous phase, or by carrying out the reaction at 60 degrees C/120 bar. All of these modifications led to an apparent rate increase in the desired allylation. A range of substituted benzaldehydes afforded the corresponding homoallylic alcohols in moderate to high yields. The presence of water constituted a necessary condition for efficient product formation, while CO2 provided an appropriate phase for clean product separation by exploiting a favorable homoallylic alcohol enrichment. In this way, 0.025 mol of homoallylic alcohol product could be isolated from the CO2 phase in 1 h, avoiding further extraction stages that would typically require organic solvents.
引用
收藏
页码:1280 / 1288
页数:9
相关论文
共 62 条
[1]   Metal mediated solvent free synthesis of homoallylic alcohols [J].
Andrews, PC ;
Peatt, AC ;
Raston, CL .
GREEN CHEMISTRY, 2001, 3 (06) :313-315
[2]   Multiphase catalysis using water-soluble metal complexes in supercritical carbon dioxide [J].
Bhanage, BM ;
Ikushima, Y ;
Shirai, M ;
Arai, M .
CHEMICAL COMMUNICATIONS, 1999, (14) :1277-1278
[3]   Heck reactions using water-soluble metal complexes in supercritical carbon dioxide [J].
Bhanage, BM ;
Ikushima, Y ;
Shirai, M ;
Arai, M .
TETRAHEDRON LETTERS, 1999, 40 (35) :6427-6430
[4]   Recovery of organic products from ionic liquids using supercritical carbon dioxide [J].
Blanchard, LA ;
Brennecke, JF .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2001, 40 (01) :287-292
[5]   Maximising opportunities in supercritical chemistry:: the continuous conversion of levulinic acid to γ-valerolactone in CO2 [J].
Bourne, Richard A. ;
Stevens, James G. ;
Ke, Jie ;
Poliakoff, Martyn .
CHEMICAL COMMUNICATIONS, 2007, (44) :4632-4634
[6]   Inverted supercritical carbon dioxide/aqueous biphasic media for rhodium-catalyzed hydrogenation reactions [J].
Burgemeister, Katja ;
Francio, Giancarlo ;
Gego, Volker H. ;
Greiner, Lasse ;
Hugl, Herbert ;
Leitner, Walter .
CHEMISTRY-A EUROPEAN JOURNAL, 2007, 13 (10) :2798-2804
[7]   Analysis of the reactions used for the preparation of drug candidate molecules [J].
Carey, John S. ;
Laffan, David ;
Thomson, Colin ;
Williams, Mike T. .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2006, 4 (12) :2337-2347
[8]  
Cenci S. M., 2012, RECENT PAT CATAL, V1, P2
[9]   Ultrasound-induced emulsification of subcritical carbon dioxide/water with and without surfactant as a strategy for enhanced mass transport [J].
Cenci, Steven M. ;
Cox, Liam R. ;
Leeke, Gary A. .
ULTRASONICS SONOCHEMISTRY, 2014, 21 (01) :401-408
[10]  
Chen D, 2012, HANDBOOK ON APPLICATIONS OF ULTRASOUND: SONOCHEMISTRY FOR SUSTAINABILITY, P1