Photochemical reactions of alkyl phenylglyoxylates

被引:58
|
作者
Hu, SK [1 ]
Neckers, DC [1 ]
机构
[1] BOWLING GREEN STATE UNIV,CTR PHOTOCHEM SCI,BOWLING GREEN,OH 43403
来源
JOURNAL OF ORGANIC CHEMISTRY | 1996年 / 61卷 / 18期
关键词
D O I
10.1021/jo960685e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Three new photoproducts, ethyl O-benzoyl mandelate (5a), ethyl O-acetylmandelate (6a), and biphenyl triketone (7a) are isolated and identified in the reactions of ethyl phenylglyoxylate (la) in benzene. Quantum yields and initial rate constants of product formation are shown to be concentration dependent. For the formation of carbonyl product 3 at lower starting material concentrations (<0.01 M), quantum yields greater than 1 are observed. Variations in the quantum yields as a function of reaction time are due to the accumulation of alpha-hydroxyphenyl ketene (D). The relative reactivities of triplet excited states of phenylglyoxylates 1 and phenyl ketones are compared. A mechanism involving both intramolecular gamma-H abstraction and intermolecular H abstraction, which leads to radical chain reaction, is proposed. Rate constants for intramolecular gamma-H abstraction (k(N)) and intermolecular H abstraction (k(I)) of methyl phenylglyoxylate (Id) are measured.
引用
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页码:6407 / 6415
页数:9
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