Journal of Organic Chemistry 2004-01-23

Facile preparation of beta-fluoro amines by the reaction of aziridines with potassium fluoride dihydrate in the presence of Bu4NHSO4.

Ren-Hua Fan, Yong-Gui Zhou, Wan-Xuan Zhang, Xue-Long Hou, Li-Xin Dai

Index: J. Org. Chem. 69(2) , 335-8, (2004)

Full Text: HTML

Abstract

Potassium fluoride combined with tetrabutylammonium bisulfate is an efficient reagent to convert a variety of aziridines derived from cyclic and acyclic alkenes to beta-fluoro amine derivatives in high yield.


Related Compounds

Related Articles:

[Chromatographia 28 , 179, (1989)]

Convenient source of 'naked'fluoride: tetra-n-butylammonium chloride and potassium fluoride dihydrate. Carpino LA and Sau AC.

[J. Chem. Soc. Chem. Commun. 11 , 514-515, (1979)]

Hydrogen Bonding in Potassium Fluoride Dihydrate: A Crystallographic, Spectroscopic, and Theoretical Study. Preisinger A, et al.

[Inorg. Chem. 33(21) , 4774-4780, (1994)]

Efficient halogenation of unsaturated organoaluminum compounds with sulfonyl halides. Ramazanov IR, et al.

[Russ. J. Org. Chem. 49(3) , 321-326, (2013)]

More Articles...