135582-19-3Relevant academic research and scientific papers
A convenient synthesis of methyl 1-alkoxy-3-perfluoroalkyl-2-naphthoates
Ding,Pu,Zhang
, p. 635 - 637 (2007/10/02)
Methyl 1-alkoxy-3-perfluoroalkyl-2-naphthoates 5 were synthesized by heating appropriately substituted 2-triphenylphosphoranylidene-2-butenoates 3 in xylenes at 250°C in a sealed tube. Compounds 3 were obtained via an intramolecular Wittig reaction of 2-alkoxycarbonylbenzyltriphenylphosphonium bromide (1) with methyl 2-perfluoroalkynoates 2 in the presence of potassium carbonate.
Stereoselective Synthesis of (Z)-Methyl 3-Perfluoroalkyl-4-substituted-phenylbutenoates
Weiyu, Ding,Jiaqi, Pu,Chunming, Zhang,Weiguo, Cao
, p. 1369 - 1373 (2007/10/02)
The stereoselective synthesis of (Z)-methyl 3-perfluoroalkyl-4-substituted-phenylbut-3-enoates 8a-o has been investigated.The reaction of substituted benzyltriphenylphosphonium bromides 5a-e with methyl 2-perfluoroalkylnoates 2a-c in the presence of K2CO3 at room temp. gives two adducts, methyl 3-perfluoroalkyl-4-substituted-phenyl-2-triphenylphosphoranylidenebut-3-enoates, 6a-o and methyl 3-perfluoroalkyl-4-substituted-phenyl-4-triphenylphosphoranylidenebut-2-enoates, 7a-o.Compounds 6a-o exist as pairs of E/Z isomers, the ratios are 2:1 for RF = CF3, and 3:1 for RF = C2F5 or C3F7.Compounds 7a-o are transformed into 6a-o when heated. (Z)-Methyl 3-perfluoroalkyl-4-substituted-phenylbut-3-enoates 8a-o can be obtained stereoselectively in high yield when an aqueous methanol solution of mixed 6a-o and 7a-o was heated for 10-20 h.
