Author:
Griffiths PG,Moad G,Rizzardo E
Abstract
A versatile free-radical
trapping agent, 1,1,3,3-tetramethylisoindolin-2-yloxyl, has been prepared from
N-benzylphthalimide by reaction with 'methylmagnesium iodide' in refluxing toluene followed by
hydrogenolysis and oxidation. The Grignard reaction
gives 2-benzyl-1,1,3,3-tetramethylisoindoline along with a small proportion of
an unexpected by-product, 2-benzyl-1-ethyl-1,3,3-trimethyliso-indoline.
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