- Synthese de 3-perfluoroalkylprop-1-enes RF-CH2-CH=CH2
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The reactions of perfluoroalkyl iodides with allylbromide or chloride, in the presence of solid potassium hydroxide KOH give 3-perfluoroalkylprop-1-enes RFCH2CH=CH2 in good yields under mild conditions. This reaction represents a synthetically viable and convenient route to such compounds.
- Rubio,Blancou,Commeyras
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p. 171 - 175
(2007/10/03)
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- Reaction of Perfluoroalkanesulfinates with Allyl and Propargyl Halides. A Convenient Synthesis of 3-(Perfluoroalkyl)prop-1-enes and 3-(Perfluoroalkyl)allenes
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The reaction of perfluoroalkanesulfinates, RfCF2SO2Na, with allyl and propargyl halides, in the presence of (NH4)2S2O8, gave 3-(perfluoroalkyl)prop-1-enes (RfCH2CH=CH2) and 3-(perfluoroalkyl)allenes (RfCH=C=CH2), respectively, in good yield.Evidence is presented for a radical addition-elimination mechanism for the reaction.The reaction represents a synthetically viable and convenient route to such compounds.
- Hu, Chang-Ming,Qing, Feng-Ling,Huang, Wei-Yuan
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p. 2801 - 2804
(2007/10/02)
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- Effect of a Perfluoroalkyl Group on the Elimination and Substitution Reactions of Two Homologous Series of Perfluoroalkyl-Substituted Iodoalkanes
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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.
- Brace, Neal O.,Marshall, Lawrence W.,Pinson, Carol J.,Wingerden, Gail van
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p. 2361 - 2368
(2007/10/02)
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