Synthesis 2003(7): 1009-1011
DOI: 10.1055/s-2003-39173
SHORTPAPER
© Georg Thieme Verlag Stuttgart ˙ New York

Base-Mediated Syntheses of New 6,6′-Di(polyfluoroalkoxy)-2,2′-Bipyridines with 100% Regioselectivity

Rajendra P. Singh, Gary V. Eggers, Jean’ne M. Shreeve*
Department of Chemistry, University of Idaho, Moscow, ID 83844-2343, USA
Fax: 208(885)9146; e-Mail: jshreeve@uidaho.edu;
Further Information

Publication History

Received 20 December 2002
Publication Date:
09 May 2003 (online)

Abstract

Reactions of N,N-difluoro-2,2′-bipyridinium bis(tetrafluoroborate) (MEC-31) (1) with fluorinated alcohols RfOH [Rf = CF3CH2, CH2FCH2, CF3CF2CH2, CHF2CF2CH2, (CF3)2CH] 2a-e, in the presence of a base at 70 °C without solvent, gave good yields of 6,6′-di(polyfluoroalkoxy)-2,2′-bipyridines 3a-e with 100% regioselectivity. Triethylamine with 1, produced 6,6′-difluoro-2,2-bipyridine (4).