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Preparation, X-ray structure, and reactivity of 2-iodylpyridines: recyclable hypervalent iodine(V) reagents.

Authors :
Yoshimura A
Banek CT
Yusubov MS
Nemykin VN
Zhdankin VV
Source :
The Journal of organic chemistry [J Org Chem] 2011 May 20; Vol. 76 (10), pp. 3812-9. Date of Electronic Publication: 2011 Apr 14.
Publication Year :
2011

Abstract

2-Iodylpyridine and four examples of 3-alkoxy-2-iodylpyridines were prepared by oxidation of the respective 2-iodopyridines with 3,3-dimethyldioxirane. Structures of 2-iodylpyridine, 2-iodyl-3-isopropoxypyridine, and 2-iodyl-3-propoxypyridine were established by single-crystal X-ray diffraction analysis. 2-Iodyl-3-propoxypyridine has moderate solubility in organic solvents (e.g., 1.1 mg/mL in acetonitrile) and can be used as a recyclable reagent for oxidation of sulfides and alcohols. The reduced form of this reagent, 2-iodo-3-propoxypyridine, can be effectively separated from the reaction mixture by treatment with diluted sulfuric acid and recovered from the acidic aqueous solution by adding aqueous sodium hydroxide.

Details

Language :
English
ISSN :
1520-6904
Volume :
76
Issue :
10
Database :
MEDLINE
Journal :
The Journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
21462949
Full Text :
https://doi.org/10.1021/jo200163m