152531-75-4Relevant articles and documents
Preparation, crystal structures, and spectroscopic and chemical properties of 2,4,6-trifluorophenyl-or 4-(methoxycarbonyl)-Phenyl-substituted (E)-1-(3-guaiazulenyl)ethylene and (2E,4E)-1-(3-guaiazulenyl)-1,3-butadiene derivatives
Takekuma, Shin-Ichi,Matsuoka, Hiroto,Ogawa, Syoutarou,Shibasaki, Yasutaka,Minematsu, Toshie
experimental part, p. 1248 - 1263 (2011/01/10)
Wittig reactions in general provide a mixture of E and Z geometric isomers, while reactions of 2,4,6-trifluorobenzaldehyde [and (E)-3-(2,4,6- trifluorophenyl)propanal] with the Wittig reagent (3-guaiazulenyl) triphenylphosphonium bromide in ethanol containing NaOEt at 25 °C for 24 h under argon give only new E (and 2E,4E)-forms selectively, i.e., (E)-1-(3-guaiazulenyl)-2-(2,4,6-trifluorophenyl)ethylene and (2E,4E)-1-(3-guaiazulenyl)-4-(2,4,6-trifluorophenyl)-1,3-butadiene. For comparative purposes, Wittig reactions of methyl 4-formylbenzoate, 4-(dimethylamino)benzaldehyde, methyl 4-[(E)-2-formylethenyl]benzoate, and (E)-3-[4-(dimethylamino)phenyl]propanal: namely, possessing an electronwithdrawing (-COOCH3) {or an electron-donating [-N(CH 3)2]} group at the C-4 position of the benzene ring, with (3-guaiazulenyl)triphenylphosphonium bromide in methanol (or ethanol) containing NaOMe (or NaOEt) at 25°C for 24h under argon afford a mixture of the corresponding geometric isomers respectively. Along with spectroscopic properties and crystal structures of the isolated products, the chemical behavior of those products toward 1,1,2,2-tetracyanoethylene (TCNE) in benzene at 25°C for 24 h under argon is reported with a view to comparative study.
