期刊
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 19, 期 -, 页码 212-216出版社
BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.19.20
关键词
Friedel-Crafts acylation; homogeneous catalysis; ionic liquids; iron catalysis; TAAILs
We have developed a robust catalyst system for the Friedel-Crafts acylation of benzene derivatives in tunable aryl alkyl ionic liquids (TAAILs), by optimizing the metal salt, reaction conditions, and ionic liquids. This system tolerates different electron-rich substrates under ambient atmosphere and allows for a multigram scale.
An iron(III) chloride hexahydrate-catalyzed Friedel-Crafts acylation of benzene derivatives in tunable aryl alkyl ionic liquids (TAAILs) has been developed. Through optimization of the metal salt, reaction conditions and ionic liquids, we were able to design a robust catalyst system that tolerates different electron-rich substrates under ambient atmosphere and allows for a multigram scale.
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