Allyl methacrylate, oxidation

Allylic intermediate, 27 185-187 ii-Allylic nickel intermediates, 33 15-18, 22 Allylic oxidation, see Oxidation, allylic Allylic species, 30 21 formation, isomerization, 30 18-19 free allyl radicals, 30 149 a-hydrogen abstraction, 30 147 Allyl methacrylate oxidation, 41 305 Allyls... 

The oxidations of C5-C8 olefins, allyl chloride, allyl alcohol, and allyl methacrylate with H202 give the corresponding epoxides. Data characterizing oxidations carried out in methanol solvent at an olefin concentration of 0.90 M, in the presence of TS-1 (6.2 g/L), are given in Table V. 

Magnesium oxide, magnesium hydroxide, calcium hydroxide, epoxy compounds, lead compounds Allylic, methacrylate... 

Synthesis of PIB prepolymers. fm-Chlorine-telechelic PIB (Mn=4,000 MVf/Mn 1.09) (7), and an allyl-telechelic PIB (Mn=9,500 Mw/Mn 1.14) (7,8) were prepared by living carbocationic polymerizations. The tert-chlorine ended PIB was quantitatively dehydrochlorinated (9) to -C(CH3)=CH2 terminated polymer. Both olefin-telechelic PIBs were then hydroborated and oxidized (10) to prepare the primary hydroxyl termini. The hydroxyl-telechelic polymers were esterified with methacryloyl chloride to methacrylate-telechelic PIBs, MA-PIB-MA (11). 

A detailed study of the mechanism of the insertion reaction of monomer between the metal-carbon bond requires quantitative information on the kinetics of the process. For this information to be meaningful, studies should be carried out on a homogeneous system. Whereas olefins and compounds such as Zr(benzyl)4 and Cr(2-Me-allyl)3, etc. are very soluble in hydrocarbon solvents, the polymers formed are crystalline and therefore insoluble below the melting temperature of the polyolefine formed. It is therefore not possible to use olefins for kinetic studies. Two completely homogeneous systems have been identified that can be used to study the polymerization quantitatively. These are the polymerization of styrene by Zr(benzyl)4 in toluene (16, 25) and the polymerization of methyl methacrylate by Cr(allyl)3 and Cr(2-Me-allyl)3 (12)- The latter system is unusual since esters normally react with transition metal allyl compounds (10) but a-methyl esters such as methyl methacrylate do not (p. 270) and the only product of reaction is polymethylmethacrylate. Also it has been shown with both systems that polymerization occurs without a change in the oxidation state of the metal. 

The rate constants for oxidation of a series of cycloalkenes with ozone have been determined using a relative rate method. The effect of methyl substitution on the oxidation of cycloalkenes and formation of secondary organic aerosols has been analysed.155 Butadiene, styrene, cyclohexene, allyl acetate, methyl methacrylate, and allyl alcohol were epoxidized in a gas-phase reaction with ozone in the absence of a catalyst. With the exception of allyl alcohol, the yield of the corresponding epoxide ranged from 88 to 97%.156 Kinetic control of distereoselection in ozonolytic lactonization has been (g) reported in the reaction of prochiral alkenes.157... 

Acetals result from oxidative coupling of alcohols with electron-poor terminal olefins followed by a second, redox-neutral addition of alcohol [11-13]. Acrylonitrile (41) is converted to 3,3-dimethoxypropionitrile (42), an intermediate in the industrial synthesis of thiamin (vitamin Bl), by use of an alkyl nitrite oxidant [57]. A stereoselective acetalization was performed with methacrylates 43 to yield 44 with variable de [58]. Rare examples of intermolecular acetalization with nonactivated olefins are observed with chelating allyl and homoallyl amines and thioethers (45, give acetals 46) [46]. As opposed to intermolecular acetalizations, the intramolecular variety do not require activated olefins, but a suitable spatial relationship of hydroxy groups and the alkene[13]. Thus, Wacker oxidation of enediol 47 gave bicyclic acetal 48 as a precursor of a fluorinated analogue of the pheromone fron-talin[59]. 

Another advantage of dendrimer-based catalysts concerns their easy recovery by stabilization at the surface of a polymer. The principal activities in dendritic catalysis lie in homogeneous catalysis, including Kharash addition of CC14 to methacrylate, palladium-catalyzed allylic alkylation, hydrogenation of olefins, hydroformylation, cyclopropanation, and oxidation.258 Dendrimers with redox-active cores have been proposed as promising materials for miniaturized information-storage circuits.259... 

Allylic oxidation (i) propene to acrolein or acrylic acid and (ii) isobutene to methacrolein or methacrylic acid the synthesis of the acids may be effected in a single step, but commercially a two-step process is used due to its better selectivity. 

Vapor-phase aerobic oxidations of lower olefins, e. g. propylene to acrolein or acrylic acid and isobutene to methacrolein or methacrylic acid, are well-established bulk chemical processes [1,2], They are usually performed over oxidic catalysts, such as bismuth molybdate or heteropoly compounds, although the scope of these allylic oxidations is limited to olefins that cannot form 1,3-dienes via oxidative dehydrogenation. Thus 1- and 2-butene are converted to butadiene, and methylbutenes to isoprene, and with higher olefins complex mixtures result from further oxidation. Hence, such methodologies are not relevant in the context of fine chemicals. 

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