Efficient synthesis of 4-methyl-1,10-phenanthroline starting from 8- aminolepidine

Article abstract of DOI:10.1080/00397919908085754

8-aminolepidine 2 reacted with glycerol 3 in presence of sodium iodide and gave 4-methyl-1,10-phenanthroline 1 with a 66 % yield.

Full text of DOI:10.1080/00397919908085754

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Efficient Synthesis of 4-Methyl-
L,10-Phenanthroline Starting
from 8-Aminolepidine
Stephane Lutun a , Eric Guichard a , Bruno Hasiak a &
Daniel Couturier a
a Laboratoire de Chimie Organique et
Environnement, Bat. C4 - Université des Sciences
et Technologies de Lille , 59655, Villeneuve d'Ascq
Cedex, France
Published online: 17 Sep 2007.
To cite this article: Stephane Lutun , Eric Guichard , Bruno Hasiak & Daniel
Couturier (1999) Efficient Synthesis of 4-Methyl-L,10-Phenanthroline Starting
from 8-Aminolepidine, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 29:2, 175-180, DOI:
10.1080/00397919908085754
To link to this article: http://dx.doi.org/10.1080/00397919908085754
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