引用本文:
Ling HE, Guo Hong TAO, Wei Shan LIU, Wei XIONG, Tao WANG, Yuan KOU. One-pot Synthesis of Lewis Acidic Ionic Liquids for Friedel-Crafts Alkylation[J]. Chinese Chemical Letters,
2006, 17(3): 321-324.
Citation: Ling HE, Guo Hong TAO, Wei Shan LIU, Wei XIONG, Tao WANG, Yuan KOU. One-pot Synthesis of Lewis Acidic Ionic Liquids for Friedel-Crafts Alkylation[J]. Chinese Chemical Letters, 2006, 17(3): 321-324.

Citation: Ling HE, Guo Hong TAO, Wei Shan LIU, Wei XIONG, Tao WANG, Yuan KOU. One-pot Synthesis of Lewis Acidic Ionic Liquids for Friedel-Crafts Alkylation[J]. Chinese Chemical Letters, 2006, 17(3): 321-324.

One-pot Synthesis of Lewis Acidic Ionic Liquids for Friedel-Crafts Alkylation
摘要:
Novel Lewis acidic ionic liquids containing thionyl cations and chloroaluminate anions were obtained by one-pot synthesis for the first time. Their acidities were determined by acetonitrile probe on IR spectrography. The ionic liquids were used as catalyst for Friedel-Crafts alkylation of benzene and 1-dodecene. The turnovers of 1-dodecene were higher than 99%. Monoalkylbenzene selectivity was 98%, while the 2-substituent product selectivity was 45%.
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关键词:
- Ionic liquids
- / green chemistry
- / one-pot synthesis
- / Lewis acidity
- / alkylation
English
One-pot Synthesis of Lewis Acidic Ionic Liquids for Friedel-Crafts Alkylation
Abstract:
Novel Lewis acidic ionic liquids containing thionyl cations and chloroaluminate anions were obtained by one-pot synthesis for the first time. Their acidities were determined by acetonitrile probe on IR spectrography. The ionic liquids were used as catalyst for Friedel-Crafts alkylation of benzene and 1-dodecene. The turnovers of 1-dodecene were higher than 99%. Monoalkylbenzene selectivity was 98%, while the 2-substituent product selectivity was 45%.
-
Key words:
- Ionic liquids
- / green chemistry
- / one-pot synthesis
- / Lewis acidity
- / alkylation

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