Volume 17, Issue 1 pp. 22-35
Research Article
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The iodine atom transfer addition reaction (I-ATRA) initiated by AIBN: Optimization, scope and radical reaction pathways

Piotr Bałczewski

Corresponding Author

Piotr Bałczewski

Department of Heteroorganic Chemistry, Laboratory of Metallo- and Metalloido-organic Chemistry, Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, 90-363 Lódź, Sienkiewicza 112, Poland

Department of Heteroorganic Chemistry, Laboratory of Metallo- and Metalloido-organic Chemistry, Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, 90-363 Lódź, Sienkiewicza 112, PolandSearch for more papers by this author
Aldona Szadowiak

Aldona Szadowiak

Department of Heteroorganic Chemistry, Laboratory of Metallo- and Metalloido-organic Chemistry, Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, 90-363 Lódź, Sienkiewicza 112, Poland

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Tomasz Białas

Tomasz Białas

Department of Heteroorganic Chemistry, Laboratory of Metallo- and Metalloido-organic Chemistry, Centre of Molecular and Macromolecular Studies, Polish Academy of Sciences, 90-363 Lódź, Sienkiewicza 112, Poland

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First published: 30 January 2006
Citations: 14

Abstract

Optimization of reaction conditions (alkene, halide, solvent, stoichiometry, manners of the reagents addition, and reaction time) of the I-ATRA reactions involving 1-iodoalkylphosphonates was carried out. GC–MS–CI/EI analyses showed main and side products of this reaction and the corresponding radical reaction pathways leading to products derived from phosphorus and nonphosphorus containing iodides, as well as explained the source of hydrogen in radical reduction processes accompanying the I-ATRA reaction. Synthesis of some 3-iodoalkyl and 3-iodoalkenylphosphonates was also presented based on the optimized procedure. © 2006 Wiley Periodicals, Inc. Heteroatom Chem 17:22–35, 2006; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20187

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