2015
DOI: 10.1515/chempap-2015-0067
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Efficient synthesis of glutaric acid from L-glutamic acid via diazoniation/hydrogenation sequence

Abstract: The practical synthetic preparation of glutaric acid has remained a major challenge to date. In the present study, glutaric acid was synthesised by way of one-pot diazoniation/hydrogenation of the readily available L-glutamic acid under aqueous conditions on a gram-scale with good yields. This is the first example of the deamination of the aliphatic primary amine via diazoniation and could afford a practical approach to the production of glutaric acid.

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Cited by 2 publications
(1 citation statement)
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“…The deamination of aromatic amines is a widely used process in the chemical industry [ 12 ]. Despite the fact that there are a variety of deamination processes, deamination of aromatic amines normally involves activating the amino group by diazotization, followed by the replacement of the diazo group with hydrogen [ 13 15 ].…”
Section: Introductionmentioning
confidence: 99%
“…The deamination of aromatic amines is a widely used process in the chemical industry [ 12 ]. Despite the fact that there are a variety of deamination processes, deamination of aromatic amines normally involves activating the amino group by diazotization, followed by the replacement of the diazo group with hydrogen [ 13 15 ].…”
Section: Introductionmentioning
confidence: 99%