Fluorination of nitrogen-containing aromatics with xenon difluoride
โ Scribed by S.P. Anand; Robert Filler
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 295 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0022-1139
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โฆ Synopsis
Pyridine reacts with xenon difluoride to give a mixture of 2-fluoropyridine, 3-fluoropyridine, and 2,6_difluoropyridine, while 8-hydroxyquinoline is converted to 5-fluoro-8-quinolinol. Aniline and benzylamine react vigorously with XeF, to yield mixtures of monofluoro isomers derived from the parent amines.
๐ SIMILAR VOLUMES
Direct fluorination of the pymole ring with electron-withdrawing gtmym, such as, -CHO, -COR, -COOR, -CON&, using xctm difluoride under mild conditions leads to the comsponding flwtopymAcs in 2544% yields. It was found that fluorination takes place only at the u-position of the pyrrole even when the