74701-31-8Relevant academic research and scientific papers
Perfluoroalkylations and perfluorooxaalkylations. Part 4. Conversion of aryl perfluoroalkanes to aryl perfluoroalkyl ketones
Chen, Grace J.,Chen, Loomis S.,Eapen, Kalathil C.
, p. 173 - 180 (2007/10/03)
The hydrolysis of benzylic fluorines with hydrobromic acid in glacial acetic acid has been utilized to convert some substituted phenyl perfluoroalkanes to the corresponding ketones.Electron-donating substituents such as -OMe, -OH or -NH2 on the benzene ri
Effect of a Perfluoroalkyl Group on the Elimination and Substitution Reactions of Two Homologous Series of Perfluoroalkyl-Substituted Iodoalkanes
Brace, Neal O.,Marshall, Lawrence W.,Pinson, Carol J.,Wingerden, Gail van
, p. 2361 - 2368 (2007/10/02)
Substitution and elimination reactions of two homologous series of compounds, induced by strong bases, were studied in aqueous alcohol and anhydrous methanol solution.Series I compounds, RF(CH2)nI having n = 2 (RF = a perfluoroalkyl group, also named an F-alkyl group), gave only RFCH=CH2 under all conditions.By contrast, RF(CH2)3Igave 4-10 times as much substitution as elimination products.Isomerization of RFCH2CH=CH2 (6) to RFCH=CHCH3 (7) occurred; this result may account, in part, for the extremely high 7/6 alkene ratios (37-81/1) obtained from elimination reactions of RFCH2CHICH3.All series II compounds, RFCH2CHI(CH2) nCH3 (n = 0-5), gave entirely elimination, and principally toward the RF group.E/Z isomer ratios varied from 2.65 to 5.These results were compared to those obtained from 1- and 2-iodooctane under the same conditions.A practical synthesis of CF3(CF2)5CH2CH2CH2I is described; the isomeric (F-alkyl)propenes 6 and 7 were also separately prepared.Rates of reactions under standard conditions for both series I and II compounds were measured.Kinetically, only second-order processes were observed, but a sharp break occurred in rate as the RF group was separated more than two carbons from the departing iodine atom, in series I compounds.Series II compounds reacted about one-tenth as fast as series I compounds.These results are discussed in the context of previous work with F-alkyl-substituted compounds.
