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HERO ID
2343262
Reference Type
Journal Article
Title
The role of labile products of styrene epoxide conversion in its oxidation in polar acid medium
Author(s)
Petrov, LV; Solyanikov, VM
Year
2013
Is Peer Reviewed?
1
Journal
Petroleum Chemistry
ISSN:
0965-5441
EISSN:
1531-8532
Volume
53
Issue
5
Page Numbers
326-330
Language
English
DOI
10.1134/S0965544113040105
Web of Science Id
WOS:000324501300007
Abstract
Phenylacetaldehyde (PAA) and benzyl alcohol (BAl) are formed in oxygen atmosphere from styrene epoxide in the presence of p- toluenesulfonic acid (TSA) in a solution of 90 vol % tert-butanol with 10 vol % chlorobenzene (BUC). The ratio of the propagation (k (2) ) to the termination (k (6)) rate constants has been measured to be k (2)/aek (6) = 8.6 x x 10(-3) (L/(mol s))(1/2) at 343 K by the method of initiated oxidation of PAA in a BUC solution. One of the products of the radical chain PAA oxidation is BA. This reaction leads to BAl accumulation during the conjugated oxidation of PAA with the epoxide in an acid alcohol medium. The contribution of BAl formed to the oxidation is almost unnoticeable.
Keywords
styrene epoxide; p-toluenesulfonic acid; phenylacetaldehyde; benzaldehyde; benzyl alcohol; oxidation by molecular oxygen
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