A facile synthesis of fluorinated alkoxytrimethylsilanes using 1-methylimidazole as an acid scavenger

Authors
Lee, BoraKim, Jin HyungLee, HyunjooAhn, Byoung SungCheong, MinserkKim, Hoon SikKim, Honggon
Issue Date
2007-02
Publisher
ELSEVIER SCIENCE SA
Citation
JOURNAL OF FLUORINE CHEMISTRY, v.128, no.2, pp.110 - 113
Abstract
Fluorinated alkoxytrimethylsilanes (R1CH2OSiMe3), potential candidates for the third-generation cleaning agents, were synthesized in high yields over 95% from the reaction of chlorotrimethylsilane and fluorinated alcohol (R1CH2OH) in the presence of 1-methylimidazole. Elemental and H-1 NMR spectroscopic analysis showed that the reaction proceeds through the formation of an intermediate, 3-methyl-1-trimethylsilylimidazolium chloride. (c) 2006 Elsevier B.V. All rights reserved.
Keywords
CFC; SILICON; CFC; SILICON; chlorofluorohydocarbons; fluorinated alkoxytrimethylsilanes; CFC alternatives; 1-methylimidazolium chloride; ionic liquids
ISSN
0022-1139
URI
https://pubs.kist.re.kr/handle/201004/134704
DOI
10.1016/j.jfluchem.2006.10.008
Appears in Collections:
KIST Article > 2007
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