Synthesis of Biobased Succinonitrile from Glutamic Acid and Glutamine

被引:48
|
作者
Lammens, Tijs M. [1 ]
Le Notre, Jerome [1 ]
Franssen, Maurice C. R. [2 ]
Scott, Elinor L. [1 ]
Sanders, Johan P. M. [1 ]
机构
[1] Wageningen Univ, NL-6700 AA Wageningen, Netherlands
[2] Wageningen Univ, Organ Chem Lab, NL-6703 HB Wageningen, Netherlands
关键词
biomass; catalysis; palladium; renewable resources; waste prevention; PRIMARY AMIDES; AMINO-ACIDS; NITRILES; SUZUKI; DEHYDRATION; COMPLEXES; CATALYSTS;
D O I
10.1002/cssc.201100030
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Succinonitrile is the precursor of 1,4-diaminobutane, which is used for the industrial production of polyamides. This paper describes the synthesis of biobased succinonitrile from glutamic acid and glutamine, amino acids that are abundantly present in many plant proteins. Synthesis of the intermediate 3-cyanopropanoic amide was achieved from glutamic acid 5-methyl ester in an 86 mol% yield and from glutamine in a 56 mol% yield. 3-Cyanopropanoic acid can be converted into succinonitrile, with a selectivity close to 100% and a 62% conversion, by making use of a palladium(II)-catalyzed equilibrium reaction with acetonitrile. Thus, a new route to produce biobased 1,4-diaminobutane has been discovered.
引用
收藏
页码:785 / 791
页数:7
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