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
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