Beilstein J. Org. Chem.2025,21, 2755–2760, doi:10.3762/bjoc.21.212
GmbH, Am Brunnen 1, 5330 Fuschl am See, Austria 10.3762/bjoc.21.212 Abstract A novel route to the flavor enhancer ethylmaltol, a synthetic 4-pyrone, from naturally abundant maltol is disclosed. Two strategies were explored for the required C1 homologation. The most direct approach, C–C bond formation
synthesis of ethylmaltol from a renewable precursor.
Keywords: ethylmaltol; flavor enhancer; maltol; methylation; 4-pyrones; Introduction
In 1969, a Pfizer patent first disclosed ethylmaltol (1) as a powerful, purely synthetic flavor and aroma enhancer (Scheme 1a) [1]. It has been found to have a 6-times
higher flavor-enhancing power compared to its naturally occurring congener maltol (2), which has a more caramel-like odor compared to the fruitier ethylmaltol (1). Owing to its strong ability to enhance the taste and odor of food, ethylmaltol (1) is used as an additive in a wide range of beverages
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Graphical Abstract
Scheme 1:
Importance and synthetic approaches to ethylmaltol (1). (a) Ethylmaltol (1) is widely used as a fla...