Organic Reactions in Ionic Liquids:An Efficient Method for the Synthesis of Phenacyl Esters by Reaction of Carboxylic Acids with α-Bromoacetophenone Promoted by Potassium Fluoride

Yi HU Jue CHEN Zhang Gao LE Zhen Chu CHEN Qin Guo ZHENG

引用本文: Yi HU,  Jue CHEN,  Zhang Gao LE,  Zhen Chu CHEN,  Qin Guo ZHENG. Organic Reactions in Ionic Liquids:An Efficient Method for the Synthesis of Phenacyl Esters by Reaction of Carboxylic Acids with α-Bromoacetophenone Promoted by Potassium Fluoride[J]. Chinese Chemical Letters, 2005, 16(7): 903-905. shu
Citation:  Yi HU,  Jue CHEN,  Zhang Gao LE,  Zhen Chu CHEN,  Qin Guo ZHENG. Organic Reactions in Ionic Liquids:An Efficient Method for the Synthesis of Phenacyl Esters by Reaction of Carboxylic Acids with α-Bromoacetophenone Promoted by Potassium Fluoride[J]. Chinese Chemical Letters, 2005, 16(7): 903-905. shu

Organic Reactions in Ionic Liquids:An Efficient Method for the Synthesis of Phenacyl Esters by Reaction of Carboxylic Acids with α-Bromoacetophenone Promoted by Potassium Fluoride

摘要: An efficient method is reported for the synthesis of phenacyl esters by reaction of carboxylic acids with α-bromoacetophenone promoted by potassium fluoride in ionic liquid[Bmim]PF6, the yield of the reaction is almost quantitative and the products are essentially pure.

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  • 收稿日期:  2004-08-16
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