- Aerosol Direct Fluorination: Alkyl Halides. 2. Chlorine Shift and the Stability of Radicals
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Unlike alkyl bromides and iodides, alkyl chlorides are shown to be stable to direct fluorination, even under ultraviolett irradiation, at temperatures of 30 deg C and below.Although less reactive than the bromides and iodides, F-alkyl chlorides may be derivatized, presenting another example of direct fluorination-survivable functionality.High (63 percent) to moderate (32 percent) isolated yields of the analogous perfluororalkyl chlorides can be synthesized by aerosol direct fluorination of 1-chloropropane, 1-chlorobutane, 1-chloro-2-methylpropane, 1-chloro-3-methylbutane, 1-chlo-ro-2-methylbutane, and chlorocyclopentane with generally less than 20 percent C-C bond cleavage.Tertiary alkyl chlorides generally undergo intramolecular 1,2-chloride shift in the earliest stages of reaction in a manner characteristic of β-chloro radicals forming principally primary F-alkyl chlorides.Thus 2-chloro-2-methylpropane produces 1-chloro-F-2-methylpropane (47 percent), and 2-chloro-2-methylbutane produces a 16:6.3:1 ratio of 1-chloro-F-2-methylbutane, 1-chloro-F-3-methylbutane, and 2-chloro-F-3-methylbutane, respectively, in 32 percent combined yield.Secondary alkyl chlorides undergo a similar but incomplete rearrangement producing mixtures of primary and secondary F-alkyl chlorides.Thus 2-chloropropane produces a 2:1 mixture of 2-chloro-F-propane and 1-chloro-F-propane in 50 percent combined yield; 2-chlorobutane produces a 1:1.5 mixture of 2-chloro-F-butane and 1-chloro-F-butane in 34 percent combined yield, and 3-chloropentane produces a 2:3:1 mixture of 3-chloro-F-pentane, 2-chloro-F-pentane, and 1-chloro-F-pentane, respectively, in a combined yield of 30 percent.Because secondary alkyl chlorides partially rearrange but primary alkyl chlorides donot rearrange at all on fluorination, doubt is cast on the postulate that the intermediate radicals are equilibrating.
- Adcock, James L.,Evans, William D.
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p. 2719 - 2723
(2007/10/02)
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- THERMOLYSE DES HALOGENURES DE PERFLUOROALCANESULFONYLE
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Perfluoroalkanesulfonyl chlorides FSO2Cl; RF= CF3, C2F5, C4F9>, decompose thermally to give the corresponding perfluoroalkyl chlorides with evolution of SO2.The latter retards the reaction, but it is catalysed by copper which also inhibits the SO2 effect. 2-methyl-2-nitrosopropane traps the perfluoroalkyl free radicals.In the presence of a perfluoroalkyl iodide FI; R'not equal RF>, other products, RFI and RFCl, are obtained.A free radical chain-mechanism is then suggested.On the other hand, perfluorobutanesulfonyl fluoride is very stable thermally.
- Oudrhiri-Hassani, M.,Brunel, D.,Germain, A.,Commeyras, A.
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p. 491 - 504
(2007/10/02)
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