Reaction of Phthalaldehyde with Aminoethanol under Different Conditions: Products and Mechanisms of Their Formation

0385299 - ÚFCH JH 2013 RIV US eng J - Článek v odborném periodiku
Klíma, Jiří - Polášek, Miroslav - Ludvík, Jiří - Urban, Jiří
Reaction of Phthalaldehyde with Aminoethanol under Different Conditions: Products and Mechanisms of Their Formation.
Journal of Heterocyclic Chemistry. Roč. 49, č. 5 (2012), s. 1202-1209. ISSN 0022-152X. E-ISSN 1943-5193
Grant CEP: GA MŠMT ME09002
Institucionální podpora: RVO:61388955
Klíčová slova: o-phthalaldehyde * orthophthalaldehyde * glutaraldehyde
Kód oboru RIV: CG - Elektrochemie
Impakt faktor: 1.224, rok: 2012

Analysis of amino acids and very efficient disinfection procedures are based on the reaction of phthalaldehyde (OPA) with primary amines. In this contribution, aminoethanol (=kolamin) as a nitrogen-containing nucleophile was used for the investigation of its reaction mechanism with OPA performed in basic aqueous buffered media (pH 9.5), where an influence of hydration or solvation is expected, and in anhydrous acetonitrile. Depending on the detailed reaction conditions, seven products were isolated and their structures determined by NMR, mass spectrometry, and X-ray structure analysis. Reaction mechanisms are proposed, which involve hydride transfers to OPA (Cannizzaro-type reaction).
Trvalý link: http://hdl.handle.net/11104/0214601