Literature DB >> 21557494

Synthesis of biobased succinonitrile from glutamic acid and glutamine.

Tijs M Lammens1, Jérôme Le Nôtre, Maurice C R Franssen, Elinor L Scott, Johan P M Sanders.   

Abstract

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.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Year:  2011        PMID: 21557494     DOI: 10.1002/cssc.201100030

Source DB:  PubMed          Journal:  ChemSusChem        ISSN: 1864-5631            Impact factor:   8.928


  1 in total

1.  One-Step Conversion of Glutamic Acid into 2-Pyrrolidone on a Supported Ru Catalyst in a Hydrogen Atmosphere: Remarkable Effect of CO Activation.

Authors:  Satoshi Suganuma; Akihiro Otani; Shota Joka; Hiroki Asako; Rika Takagi; Etsushi Tsuji; Naonobu Katada
Journal:  ChemSusChem       Date:  2019-03-04       Impact factor: 8.928

  1 in total

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