CsOH catalyzed aerobic oxidative synthesis of p-quinols from multi-alkyl phenols under mild conditions  

CsOH catalyzed aerobic oxidative synthesis of p-quinols from multi-alkyl phenols under mild conditions

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作  者:Yu-Feng Liang Kai Wu Zhiqing Liu Xiaoyang Wang Yujie Liang Chenjiang Liu Ning Jiao 

机构地区:[1]State Key Laboratory of Natural and Biomimetic Drugs [2]School of Pharmaceutical Sciences, Peking University [3]The Key Laboratory of Oil and Gas Fine Chemicals, Ministry of Education & Xinjiang Uygur Autonomous Region, Xinjiang University

出  处:《Science China Chemistry》2015年第8期1334-1339,共6页中国科学(化学英文版)

基  金:supported by the National Natural Science Foundation of China(21325206,21172006);the Key Laboratory of Oil and Gas Fine Chemicals(XJDX0908-2013-2)

摘  要:p-Quinols are ubiquitous structural motifs of various natural products and pharmaceutical compounds,and versatile building blocks in synthetic chemistry.The reported methods for the synthesis of p-quinol require stoichiometric amounts of oxidants.Molecular oxygen is considered as an ideal oxidant due to its natural,inexpensive,and environmentally friendly characteristics.During the ongoing research of C–H bond hydroxylation,we found that multi-alkyl phenols could react with molecular oxygen under mild conditions.Herein,we describe an efficient oxidative de-aromatization of multi-alkyl phenols to p-quinols.1 atm of molecular oxygen was used as the oxidant.Many multi-alkyl phenols could react smoothly at room temperature.Isotopic labeling experiment was also performed,and the result proved that the oxygen atom in the produced hydroxyl group is from molecular oxygen.p-Quinols are ubiquitous structural motifs of various natural products and pharmaceutical compounds, and versatile building blocks in synthetic chemistry. The reported methods for the synthesis of p-quinol require stoichiometric amounts of oxidants. Molecular oxygen is considered as an ideal oxidant due to its natural, inexpensive, and environmentally friendly characteristics During the ongoing research of C-H bond hydroxylation, we found that multi-alkyl phenols could react with molecular oxygen under mild conditions. Herein, we describe an efficient oxidative de-aromatization of multi-alkyl phenols to p-quinols. 1 atm of molecular oxygen was used as the oxidant. Many multi-alkyl phenols could react smoothly at room temperature. Isotopic labeling experiment was also performed, and the result proved that the oxygen atom in the produced hydroxyl group is from molecular oxygen.

关 键 词:p-quinol molecular oxygen de-aromatization CARBANION cesium hydroxide 

分 类 号:O621.3[理学—有机化学]

 

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