Synthesis 2014; 46(08): 1073-1078
DOI: 10.1055/s-0033-1340843
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis, Characterization, and Crystal Structure of Sodium (Methyl α-d-Mannopyranosid)uronate Monohydrate

Peng Xu
a   NIDDK, LBC, National Institutes of Health, Bethesda, MD 20892-0815, USA   Fax: +1(301)4805703   Email: kpn@helix.nih.gov
,
Zbigniew Dauter
b   Macromolecular Crystallography Laboratory, NCI, Argonne National Laboratory, Argonne, IL 60439, USA
,
Pavol Kováč*
a   NIDDK, LBC, National Institutes of Health, Bethesda, MD 20892-0815, USA   Fax: +1(301)4805703   Email: kpn@helix.nih.gov
› Author Affiliations
Further Information

Publication History

Received: 07 January 2014

Accepted after revision: 29 January 2014

Publication Date:
19 February 2014 (online)


Abstract

TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl)-mediated oxidation of methyl α-d-mannopyranoside with sodium hypochlorite gave sodium (methyl α-d-mannopyranosid)uronate, which was obtained as a crystalline monohydrate in ~70% yield without chromatography. Its purity was proved by NMR spectroscopy, a newly developed HPLC method, combustion analysis, and X-ray crystallography. The crystal structure, solved from synchrotron diffraction data in space group P212121, revealed that the packing of the uronate molecules is connected by an extensive network of hydrogen bonds, and that the Na+ ion is coordinated by six oxygen ligands from one water and three surrounding sugar molecules.

Supporting Information

 
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