JOURNAL ARTICLE

Synthesis of [13C5] and [carbonyl‐14C]‐5‐chlorofuran‐2‐carboxylic acid

Peter N. DorffMark PowellCharles S. Elmore

Year: 2010 Journal:   Journal of Labelled Compounds and Radiopharmaceuticals Vol: 54 (3)Pages: 123-125   Publisher: Wiley

Abstract

Abstract The inventory of labeled compounds and methods for their preparation are constantly growing, but still more building blocks of biologically relevant compounds need to be developed. Furans are frequently encountered in bioactive molecules, and a good synthesis of labeled furan is found in the literature. We required a relatively uncommon labeled furan, 5‐chloro‐2‐furoic acid, for investigative work labeled with C‐13 and C‐14. Carboxylation of the lithium anion of [ 13 C 4 ]furan with 13 CO 2 followed by chlorination using benzyltrimethylammonium dichloroiodate provided the target compound in modest yield and high purity. The same procedure was then repeated with unlabeled furan and 14 CO 2 to give [carbonyl‐ 14 C]‐5‐chlorofuran‐2‐carboxylic acid. Copyright © 2010 John Wiley & Sons, Ltd.

Keywords:
Furan Carboxylation Chemistry Carboxylic acid Yield (engineering) Lithium (medication) Molecule Organic chemistry Medicinal chemistry Catalysis Materials science

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0.17
FWCI (Field Weighted Citation Impact)
12
Refs
0.52
Citation Normalized Percentile
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Citation History

Topics

Synthesis and Biological Evaluation
Physical Sciences →  Chemistry →  Organic Chemistry
Synthesis of heterocyclic compounds
Physical Sciences →  Chemistry →  Organic Chemistry
Coordination Chemistry and Organometallics
Physical Sciences →  Chemistry →  Organic Chemistry

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