Various synthetic approaches to fluoroalkyl p-nitrophenyl ethers
D Prescher, T Thiele, R Ruhmann
Index: Preschera, Dietrich; Thiele, Thomas; Ruhmann, Ralf Journal of Fluorine Chemistry, 1996 , vol. 79, # 2 p. 145 - 148
Full Text: HTML
Citation Number: 27
Abstract
Homologous 1H, 1H-perfluoroalkyl p-nitrophenyl ethers (alkyl= C2-C8) were synthesized using different methods. The results are discussed in context with contradictory comments of the literature. The fluoroalkoxylation of p-chloronitrobenzene occurs in only one step, but it is limited to small fluoroalkyl groups. The fluoroalkylation of p-nitrophenol via sulphonic acid esters is a better synthetic route. Differences in reactivity and yield between tosylates, ...
Related Articles:
[Hansen,R.L. Journal of Organic Chemistry, 1965 , vol. 30, p. 4322 - 4324]