Preparation of the E- and Z-heptafluorobutenyl-2-zinc reagent by zinc-induced dehalogenation/metallation of 2,2-dibromo-octafluorobutane
摘要:
The AlCl3-catalyzed isomerization of CF3CFBrCFBrCF3 afforded CF3CF2CBr2CF3, which upon treatment with 2 equiv. zinc in DMF underwent dehalogenation/metallation to afford a 1:1 mixture of E- and Z-CF3CF=C(ZnX)CF3 in 96% F-19 NMR yield. The zinc reagent exhibited poor thermal stability in DMF and completely decomposed by a beta-elimination route in 24 h at 60-degrees-C. However, the zinc reagent prepared from E- and Z-CF3CF=CICF3 in triglyme showed enhanced thermal stability and gave E- and Z-p-NO2C6H4C(CF3)=CFCF3 in a palladium-catalyzed coupling reaction with p-NO2C6H4I.
Preparation of the E- and Z-heptafluorobutenyl-2-zinc reagent by zinc-induced dehalogenation/metallation of 2,2-dibromo-octafluorobutane
作者:Peter A. Morken、Robert F. Campbell、Donald J. Burton
DOI:10.1016/0022-1139(93)02905-t
日期:1994.1
The AlCl3-catalyzed isomerization of CF3CFBrCFBrCF3 afforded CF3CF2CBr2CF3, which upon treatment with 2 equiv. zinc in DMF underwent dehalogenation/metallation to afford a 1:1 mixture of E- and Z-CF3CF=C(ZnX)CF3 in 96% F-19 NMR yield. The zinc reagent exhibited poor thermal stability in DMF and completely decomposed by a beta-elimination route in 24 h at 60-degrees-C. However, the zinc reagent prepared from E- and Z-CF3CF=CICF3 in triglyme showed enhanced thermal stability and gave E- and Z-p-NO2C6H4C(CF3)=CFCF3 in a palladium-catalyzed coupling reaction with p-NO2C6H4I.