Oxidation reactions aldehydes

Note that the value of EO for the ethanol/aldehyde oxidation reaction above is the same magnitude, but opposite sign of the EO value given in Table 15.1. This is because the reactions in Table 15.1 are all written as reductions ... 

Oxidation Reactions. In general, the aldehyde function is easily oxidized to form the corresponding carboxyUc acid. 

Reaction 21 is the decarbonylation of the intermediate acyl radical and is especially important at higher temperatures it is the source of much of the carbon monoxide produced in hydrocarbon oxidations. Reaction 22 is a bimolecular radical reaction analogous to reaction 13. In this case, acyloxy radicals are generated they are unstable and decarboxylate readily, providing much of the carbon dioxide produced in hydrocarbon oxidations. An in-depth article on aldehyde oxidation has been pubHshed (43). 

Reactor Configuration. The horizontal cross-sectional area of a reactor is a critical parameter with respect to oxygen mass-transfer effects in LPO since it influences the degree of interaction of the two types of zones. Reactions with high intrinsic rates, such as aldehyde oxidations, are largely mass-transfer rate-limited under common operating conditions. Such reactions can be conducted effectively in reactors with small horizontal cross sections. Slower reactions, however, may require larger horizontal cross sections for stable operation. 

Oxidation of LLDPE starts at temperatures above 150°C. This reaction produces hydroxyl and carboxyl groups in polymer molecules as well as low molecular weight compounds such as water, aldehydes, ketones, and alcohols. Oxidation reactions can occur during LLDPE pelletization and processing to protect molten resins from oxygen attack during these operations, antioxidants (radical inhibitors) must be used. These antioxidants (qv) are added to LLDPE resins in concentrations of 0.1—0.5 wt %, and maybe naphthyl amines or phenylenediamines, substituted phenols, quinones, and alkyl phosphites (4), although inhibitors based on hindered phenols are preferred. 

Rhenium oxides have been studied as catalyst materials in oxidation reactions of sulfur dioxide to sulfur trioxide, sulfite to sulfate, and nitrite to nitrate. There has been no commercial development in this area. These compounds have also been used as catalysts for reductions, but appear not to have exceptional properties. Rhenium sulfide catalysts have been used for hydrogenations of organic compounds, including benzene and styrene, and for dehydrogenation of alcohols to give aldehydes (qv) and ketones (qv). The significant property of these catalyst systems is that they are not poisoned by sulfur compounds. 

Aldehyde Hydrogen Reactions. The hydrogen of the aldehyde groupis readily oxidized to OH, forming benzoic acid [65-85-0]. 

Oxidative reactions frequently represent a convenient preparative route to synthetic intermediates and end products This chapter includes oxidations of alkanes and cycloalkanes, alkenes and cycloalkenes, dienes, aromatic fluorocarbons, alcohols, phenols, ethers, aldehydes and ketones, carboxylic acids, nitrogen compounds, and organophosphorus, -sulfur, -selenium, -iodine, and -boron compounds... 

The formation of a-acetoxyketones by oxidation of enamines with thallic acetate has been studied in detail (27) and found to be of preparative value (80 % yields) particularly in five- and six-membered-ring ketone derivatives. Enamines of linear or seven-membered-ring ketones were oxidized also, but at very much slower rates. Enamines of aldehydes with a-hydrogen substituents underwent self-eondensations during the oxidation reactions. Lead tetraacetate was less satisfactory as an oxidizing agent. 

Further oxidation of an aldehyde product to the corresponding carboxylic acid does not take place. Moreover, the SM>ern oxidation reaction does not require the use of toxic and pollutant chromium reagents. The activated DMSO species, however, are stable only at low temperature, which might in some cases be a drawback of this method. 

Much like the oxidation of propylene, which produces acrolein and acrylic acid, the direct oxidation of isobutylene produces methacrolein and methacrylic acid. The catalyzed oxidation reaction occurs in two steps due to the different oxidation characteristics of isobutylene (an olefin) and methacrolein (an unsaturated aldehyde). In the first step, isobutylene is oxidized to methacrolein over a molybdenum oxide-based catalyst in a temperature range of 350-400°C. Pressures are a little above atmospheric ... 

ThomsonNHDV, Click Organic Interactive to use a web-based palette to predict products from a variety of oxidation reactions involving aldehydes and ketones. 

At elevated temperatures, methylene carbons cleave from aromatic rings to form radicals (Fig. 7.44). Further fragmentation decomposes xylenol to cresols and methane (Fig. 7.44a). Alternatively, auto-oxidation occurs (Fig. 1.44b ). Aldehydes and ketones are intermediates before decarboxylation or decarbonylation takes place to generate cresols and carbon dioxide. These oxidative reactions are possible even in inert atmospheres due to the presence of hydroxyl radicals and water.5... 

The above-described reverse reaction (viz. the Fe-catalyzed dehydrogenation of alcohols to ketones/aldehydes) has been reported by Williams in 2009 (Table 9) [58]. In this reaction, the bicyclic complex 16 shows a sluggish activity, whereas the dehydrogenation of l-(4-methoxyphenyl)ethanol catalyzed by the phenylated complex 17 affords the corresponding ketone in 79% yield when 1 equiv. (relative to 17) of D2O as an additive was used. For this oxidation reaction, l-(4-methoxyphenyl) ethanol is more suitable than 1-phenylethanol and the reaction rate and the yield of product are higher. 

Similar kinetics are obtained with a-methylacraldehyde , but with croton-aldehyde the reaction is essentially first order in Mn(III), tending to zero-order only at relatively high [Mn(Ill)]. The oxidation of acraldehyde is viewed as a rapid reaction preceded by a slow acid-catalysed hydration, viz. 

The reductive transformation of arene carboxylates to the corresponding aldehydes under aerobic conditions has already been noted. In addition, aromatic aldehydes may undergo both reductive and oxidative reactions, with the possibility of decarboxylation of the carboxylic acid formed ... 

A reaction of practical importance is the oxidation of a carbohydrate aldehyde group to a carboxyl group. This is the basis for a process converting glucose to calcium gluconate, a substance of pharmaceutical interest. The oxidation reaction occurs at graphite electrodes in the presence of the Brj/Br" redox system. Calcium salt is added to the solution to prevent further oxidation of free gluconic acid. 

The spirobenzylisoquinoline 171b derived from berberine (15) (Section IV,A,1) was oxidized with m-chloroperbenzoic acid to the /V-oxide 389, which was treated with trifluoroacetic anhydride to afford dehydrohydrastine (370) in 56% overall yield (Scheme 71) through the Polonovski reaction (187). Holland et al. (188,189) reported the reverse reaction from dehydrophthalides to spirobenzylisoquinolines, namely, 370 was reduced with diisobutylalu-minum hydride to give a mixture of two diastereoisomeric spirobenzylisoquinolines 320 and 348 via the enol aldehyde. This reaction was applied to synthesis of various spirobenzylisoquinoline alkaloids such as (+)-sibiricine (352), ( + )-corydaine (347), (+ )-raddeanone (354), ( )-yenhusomidine (359), (+ )-ochrobirine (343), and ( )-yenhusomine (323). 

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