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Switchable-Hydrophilicity Solvents for Product Isolation and Catalyst Recycling in Organocatalysis
被引:25
|作者:
Grossehilmann, Julia
[1
]
Vanderveen, Jesse R.
[2
]
Jessop, Philip G.
[2
]
Kragl, Udo
[1
]
机构:
[1] Univ Rostock, Dept Chem, Albert Einstein Str 3a, D-18059 Rostock, Germany
[2] Queens Univ, Dept Chem, 90 Bader Lane,Chernoff Hall, Kingston, ON K7L 3N6, Canada
来源:
关键词:
catalyst recycling;
downstream processing;
microreactor;
organocatalysis;
switchable solvents;
SOLID-SUPPORTED ORGANOCATALYST;
ASYMMETRIC MICHAEL ADDITION;
CINCHONA ORGANOCATALYSTS;
HOMOGENEOUS CATALYSIS;
TUNABLE SOLVENTS;
SEPARATION;
EXTRACTION;
NANOFILTRATION;
EFFICIENT;
SYSTEMS;
D O I:
10.1002/cssc.201501654
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Switchable-hydrophilicity solvents (SHSs) are solvents that can switch reversibly between a water-miscible state to a state that forms a biphasic mixture with water. In this case study, SHSs have been studied for easy product/catalyst separation as well as catalyst recycling. A series of tertiary amine SHSs have been identified for the extraction of the hydrophilic product from the postreaction mixture. Here, we determined high extraction efficiencies for the product (>84%) and low extraction rates for the catalyst (<0.1%). With the catalyst recycling experiments, we isolated the product in high purity (>98%) without further purification steps. At the same time, the catalyst was reused without any loss of activity (>91% enantiomeric excess, >99% yield) four times. Furthermore, we optimized the extraction efficiency by working with a microextractor. In addition, with the use of a falling-film microreactor, we obtained the product with high enantioselectivity by working at ambient conditions.
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页码:696 / 702
页数:7
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