A practical and environmentally friendly protocol for synthesis of α‐deuterated carboxylic acids

An efficient method for synthesis of α-deuterated carboxylic acids from malonic acid derivatives has been developed. Hydrogen/deuterium exchange followed by decarboxylation take place in the same vessel and resulted in high isotopic purity. α-deuterated carboxylic acids have been synthesized from the corresponding malonic acids via hydrogen/deuterium exchange and decarboxylation in presence of D2O. The method is general, mild and efficient and does not require organic solvents or other additives. Yields range between 83% and 94% and purification was not necessary. Starting materials were easy accessible and the α-deuterated carboxylic acids may easily be transformed to other labeled compounds such as alcohols, aldehydes, esters, and amides. Characterization with NMR confirmed purity and isotopic purity.
Source: Journal of Labelled Compounds and Radiopharmaceuticals - Category: Biochemistry Authors: Tags: RESEARCH ARTICLE Source Type: research