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

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

^*Corresponding author for this work

College of Health and Life Sciences

Research output: Contribution to journal › Article › peer-review

Abstract

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.

Original language	English
Pages (from-to)	903-905
Number of pages	3
Journal	Chinese Chemical Letters
Volume	16
Issue number	7
Publication status	Published - 1 Jul 2005

Keywords

Ionic liquids
Phenacyl esters
Potassium fluoride

Cite this

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title = "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",

abstract = "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.",

keywords = "Ionic liquids, Phenacyl esters, Potassium fluoride",

author = "Yi Hu and Jue Chen and Le, {Zhang Gao} and Chen, {Zhen Chu} and Zheng, {Qin Guo}",

year = "2005",

month = jul,

day = "1",

language = "English",

volume = "16",

pages = "903--905",

journal = "Chinese Chemical Letters",

issn = "1001-8417",

publisher = "Elsevier",

number = "7",

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TY - JOUR

T1 - Organic reactions in ionic liquids

T2 - An efficient method for the synthesis of phenacyl esters by reaction of carboxylic acids with α- bromoacetophenone promoted by potassium fluoride

AU - Hu, Yi

AU - Chen, Jue

AU - Le, Zhang Gao

AU - Chen, Zhen Chu

AU - Zheng, Qin Guo

PY - 2005/7/1

Y1 - 2005/7/1

N2 - 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.

AB - 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.

KW - Ionic liquids

KW - Phenacyl esters

KW - Potassium fluoride

UR - http://www.scopus.com/inward/record.url?scp=33745033353&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:33745033353

SN - 1001-8417

VL - 16

SP - 903

EP - 905

JO - Chinese Chemical Letters

JF - Chinese Chemical Letters

IS - 7

ER -

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

Abstract

Keywords

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