化学
重氮甲烷
萘
苯酚
钯
催化作用
有机化学
酚类
水解
药物化学
作者
Keisuke Gondo,Juzo Oyamada,Tsugio Kitamura
出处
期刊:Organic Letters
[American Chemical Society]
日期:2015-09-24
卷期号:17 (19): 4778-4781
被引量:39
标识
DOI:10.1021/acs.orglett.5b02336
摘要
A strategy for desilylative acetoxylation of (trimethylsilyl)arenes has been developed in which (trimethylsilyl)arenes are converted into acetoxyarenes. The direct acetoxylation is performed in the presence of 5 mol % of Pd(OAc)2 and PhI(OCOCF3)2 (1.5 equiv) in AcOH at 80 °C for 17 h. The acetoxyarenes are obtained in good to high yields (67-98%). The synthetic utility is demonstrated with a one-pot transformation of (trimethylsilyl)arenes to phenols by successive acetoxylation and hydrolysis. Furthermore, desilylative acyloxylation of 2-(trimethylsilyl)naphthalene using several carboxylic acids has been conducted.
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