Abstract:Perbenzoic and peracetic acids have been used for some time to determine the degree of unsaturation and the rate of oxidation of olefinic compounds.2 Of particular interest in our investigations is the work of Bóeseken and Blumberger on the three isomeric phenylbutenes, 1,2-C6H6-CH=CH-CH2-CH3; A2'3-C6H6-CH2-CH=CH-CH3; 3,4-C6H5-CH2-CH2-CH=CH2; and also on cinnamic acid and its methyl
“…Although considerable evidence has been collected that the reaction proceeds as shown in the equation, some workers (376,511) have suggested that the peracid adds directly to the double bond, followed by splitting out of benzoic acid. This erroneous idea has found its way into a standard reference work on organic chemistry (2).…”
“…Although considerable evidence has been collected that the reaction proceeds as shown in the equation, some workers (376,511) have suggested that the peracid adds directly to the double bond, followed by splitting out of benzoic acid. This erroneous idea has found its way into a standard reference work on organic chemistry (2).…”
“…(10) Filachione, E. M., 'Lengel, J. H., and Fisher, C. H., Ibid., 37, 388 (1945). (11) Filachione, E. M., Lengel, J. H., and Fisher, C. H., J. Am.…”
Section: Literature Citedmentioning
confidence: 99%
“…The first study of perbenzoic acid addition to double bonds was made by Prileschajew (IS), but the usefulness of the reaction has been confined to the preparation of hydroxy benzoates (11,12) and epoxides (2). Other peracids-peracetic (16), percamphoric (10), and perphthalic (3)-have been used as addition reagents in syntheses.…”
Oxiranes and alpha‐glycols can be prepared from olefins by a variety of methods. One of the most important and generally applicable of these is the oxidation of ethylenic compounds with organic peracids. Depending on the peracid employed and/or operating conditions either an oxirane or an alpha‐glycol can be obtained in good yield. It is important to note that the oxidation step both in epoxidation and hydroxylation reactions with organic peracids is the conversion of the olefin to the oxirane.
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