Combining Low-Pressure CO2 Capture and Hydrogenation To Form Methanol

被引:164
作者
Khusnutdinova, Julia R. [1 ]
Garg, Jai Anand [1 ]
Milstein, David [1 ]
机构
[1] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
基金
欧洲研究理事会; 以色列科学基金会;
关键词
carbon dioxide; hydrogenation; methanol; oxazolidinone; ethanolamine; ruthenium; pincer; RUTHENIUM-CATALYZED HYDROGENATION; METAL-LIGAND COOPERATION; CARBON-DIOXIDE; HOMOGENEOUS HYDROGENATION; AMINE; MONOETHANOLAMINE; ALCOHOLS;
D O I
10.1021/acscatal.5b00194
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 paper describes a novel approach to CO2 hydrogenation, in which CO2, capture with aminoethanols at low pressure is coupled with hydrogenation of the captured product, oxazolidinone, directly to MeOH. In particular, (2-methylamino)ethanol or valinol captures CO, at 1-3 bar in the presence of catalytic Cs2CO3 to give the corresponding oxazolidinones in up to 65-70 and 90-95% yields, respectively. Efficient hydrogenation of oxazolidinones was achieved using PNN pincer Ru catalysts to give the corresponding aminoethanol (up to 95-100% yield) and MeOH (up to 78-92% yield). We also have shown that both CO2 capture and oxazolidinone hydrogenation can be performed in the same reaction mixture using a simple protocol that avoids intermediate isolation or purification steps. For example, CO2, can be captured by valinol at 1 bar with Cs2CO3 catalyst followed by 4-isopropyl-2-oxazolidinone hydrogenation in the presence of a bipy-based pincer Ru catalyst to produce MeOH in 50% yield after two steps.
引用
收藏
页码:2416 / 2422
页数:7
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