Related Experiment Video
Updated: Mar 28, 2026

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
Published on: September 6, 2019
Organocatalytic route for the synthesis of propionylated starch
S Di Filippo1, M V Tupa1, A Vázquez1
1Biotechnology and Biosynthesis Group, Institute of Technology in Polymers and Nanotechnology (ITPN), Engineering Faculty, University of Buenos Aires, Las Heras 2214 (CP 1127AAR), Buenos Aires, Argentina.
Abstract:
In recent years acetylated, propionylated and butyrylated starches have received special attention due to their capacity to deliver specific short chain fatty acids (SCFAs) to the colon in a sustained and predictable manner, and thus contribute to maintaining the normal physiologic function of the large bowel and preventing specific diseases. In the current contribution a non-conventional organocatalytic solventless route for the eco-friendly propionylation of corn starch is proposed. The catalyst used in the acylation is a naturally occurring α-hydroxy acid (l-tartaric acid). Propionylated starches with degree of substitution (DS) in the 0.05-1.59 interval were obtained and characterized in terms of chemical structure, morphology, crystallinity, thermal stability and hydrophilicity. Results showed that by the proposed methodology propionylated starch with the DS required for clinical use (i.e. 0.2-0.3) could be obtained within 2-3h of reaction. Characterization results evidenced the progressive loss of crystallinity of starch granules as higher substitution levels were conferred.
Related Concept Videos
Production of Organic Acids
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Esters to β-Ketoesters: Claisen Condensation Mechanism
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
α-Hydroxy Ketones via Reductive Coupling of Esters: Acyloin Condensation Overview

