| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5271479 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
The synthesis and spectroscopic characterization of the new phthalonitrile 5-tert-butyl-3-(trifluoromethyl)phthalonitrile is reported. A six-step route, which started with a regiospecific iodination, followed by CuI-catalyzed trifluoromethylation, is discussed. The title compound is also converted into the more reactive compound 6-tert-butyl-4-trifluoromethyl-1,3-diiminoisoindoline.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Åukasz Åapok, Arkadiusz Gut, Maria Nowakowska,