Chlorine atoms alkenes, reactions with

Notice that the addition of chlorine converts the carbon-carbon double bond into a single bond because each carbon atom now has formed a new bond with a chlorine atom. Alkenes and alkynes can also add hydrogen in hydrogenation reactions. For example, in the presence of an appropriate catalyst, propene reacts with hydrogen gas to form propane. 

Table 6.14 gives the rate constants for the reactions of chlorine atoms with some simple alkenes and some biogenic hydrocarbons. As expected, the reactions are... 

TABLE 6.14 Some Reported Values of the Rate Constants for the Reactions of Chlorine Atoms with Some Alkenes at 1 atm Total Pressure and 298 K... 

However, a computational study124 shows that the Kishi model controls the stereoselectivity for (Z)-alkenes. Note also that in the Diels-Alder reactions of hexachloropentadiene with chiral alkenes, the inside alkoxy effect is attributed to electrostatic repulsion of the oxy group in the125 outside position with the chlorine atom of hexachloropentadiene in the 1-position. 

Benzonitrile oxide (C in Figure 15.44) is an isolable 1,3-dipole. It can be generated from benzaldoxime and anNaOH/Cl2 solution. Under these reaction conditions the oxime/nitroso anion (A B) is initially formed and chlorine disproportionates into Cl—O and chloride. An SN reaction of the negatively charged C atom of the anion A B at the Cl atom of Cl— O or of Cl—O—H affords the oc-chlorinated nitroso compound E, which tautomerizes to the hydroxamic acid chloride D. From that species, the nitrile oxide C is generated via a base mediated 1,3-elimination. Isoxazoles are formed in the reactions of C with alkynes (Figure 15.44), while isoxazolines would be formed in its reactions with alkenes. 

The second problem in the addition of 1,1-dichlorodifluoroethylene to 1,3-butadiene is regiospecificity. Carbon 1 of 1,3-butadiene may become attached either to the carbon holding two chlorines or to the carbon with two fluorines. The cycloaddition of fluorinated alkenes is usually not a concerted four-center reaction in which the bonds are formed simultaneously or nearly so. Instead, the reaction is a stepwise biradical process in which the first step is formation of a free-radical intermediate with a single electron at that end of the double bond that can better accomodate it. That happens at the carbon linked to two chlorine atoms. Thus, a biradical is formed that cyclizes to form 2,2-dichloro-l,l-difluoro-3-vinylcyclobutane M [118, 119, 720]. 

Both sets of starting materials look all right—the regiochemistry is correct for the first and doesn t matter for the second. However, we prefer the second because we can control the stereochemistry by using ds-butene as the alkene and we van make the reaction work better by using dichloroketene instead of ketene itself, reducing out the chlorine atoms with zinc. 

As a striking exanqrle, photo-initiated chlorination (Scheme 21) of 3 mM (19) with 1.5 equiv. PhICb led to the 9-chloro derivative (20) in >98% yield with Ag this was converted to the A -alkene. Again the template-directed reaction overcomes the normal reactivity of the substrate, but at 21 mM (19) undirected reactions start to compete and some 6-chloro steroid is also formed. A pyridine A(-oxide template, that can use three-electron bonding to complex a chlorine to the oxygen atom, seems to be almost as effective. Furthermore, an imidazole template in compound (21) directs chlorination at C-9 with similar efficiency to the templates previously examined, and (21) is particularly easily prepared using caibonyldiimidazole. 

The ene- pe chlorination, specific with this halogen atom, of alkenes would account for a somewhat different mode of halogen addition, giving usefiil allylic dilorides. Efficient and convenient reagents and methods develtqted are dichlorine monoxide (ChO equation 36), r-butyl hypochlorite, and electro-chemical reactions with chloride ion (equation 37). The ene-type chlorination proceeds smoothly with... 

Diaiyl sulfide templates have also been used to direct chlorinations. The selectivities indicate that the chlorine atom is bound to the sulfur, but the yields are not as good as those with aryl iodide templates. The problem is that the sulfur gets oxidized under the reaction conditions. As expected, a thiophene ring is more stable to oxidation and its sulfur atom can still bind chlorine in a radical relay process." The best sulfur template so far examined is the thioxanthone system (Scheme 20). Thus with 3 equiv. PhICh compound (18) undergoes directed C-9 chlorination in 100% conversion, affording a 71% yield of the A iO-alkene sifter base treatment, along with some polar products from excessive chlorination. The thioxanthone template can be recovered unchanged. 

Substitution of hydrogen, in an alkene, by fluorine leads to increased reactivity for a number of processes for example, with tetrafluoroethene, heats of addition of chlorine, hydrogenation and polymerisation are 58.5, 66.9 and 71.1kJmol greater, respectively, than for the analogous reactions with ethene [3, 29]. These observations could be attributed either to an increase in the carbon-fluorine bond strength upon changing the hybridisation of the carbon atoms bonded to fluorine [30] or to ir-bond destabilisation by fluorine [31]. 

When metal ion complexed amino radicals are produced by the reaction of A -chloro amines with reducing metal salts in the presence of alkenes, /6-halo amines are produced12-39 41. The reaction of 1-chloropiperidine with cyclohexene, iron(II) sulfate and iron(III) chloride in methanol afforded mainly the d.s-adduct of 2. The diastereoselectivity is attributed to coordination of the unprotonated amino group with the iron(III) salt, which is mainly responsible for the chlorine atom transfer. With A-chlorodimethylarnine and 4-chloromorpholine lower yields are obtained. 

Anions of a-silyl phosphonates of type (153) also undergo additions to carbonyl compounds. The corresponding addition products, 3-silyl alkoxides, can react with ketones to yield the product of the Peterson alkenation or the Wittig reaction. In practice only the Peterson product (154) is obtained, indicating that loss of OSiMes is faster than elimination of C PPhs (Scheme 68). 72 If the a-silyl carbanion is adjacent to a chlorine atom (155), an internal displacement reaction follows the initial formation of the -silyl alkoxide, and epoxides (156) are formed (Scheme 69). 74... 

The cycloaddition of ketenes with alkenes to give cyclobutanones is a general reaction. Dimerization of the ketene is a serious side reaction with ketene itself and with monoalkyl ketenes. Dichloroketene is more reactive than simple ketenes due to the electron-withdrawing effect of the chlorine atoms and reacts readily with a wide variety of alkenes to give cyclobutanones. 

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