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・ Trifurcula graeca
・ Trifurcula hamirella
・ Trifurcula headleyella
・ Trifurcula helladica
・ Trifurcula iberica
・ Trifurcula immundella
・ Trifurcula istriae
・ Trifurcula josefklimeschi
・ Trifurcula kalavritana
・ Trifurcula lavandulae
・ Trifurcula liskai
・ Trifurcula luteola
・ Trifurcula macedonica
・ Trifurcula magna
・ Trifurcula manygoza
Trifluoromethanesulfonic acid
・ Trifluoromethanesulfonic anhydride
・ Trifluoromethanesulfonyl azide
・ Trifluoromethyl
・ Trifluoromethyl hypofluorite
・ Trifluoromethyl sulphur pentafluoride
・ Trifluoromethylaminoindane
・ Trifluoromethylation
・ Trifluoromethylisocyanide
・ Trifluoromethylphenylpiperazine
・ Trifluoromethylsulfonyl
・ Trifluoromethyltrimethylsilane
・ Trifluorooxonium
・ Trifluorotoluene
・ Trifluperidol


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Trifluoromethanesulfonic acid : ウィキペディア英語版
Trifluoromethanesulfonic acid

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Trifluoromethanesulfonic acid, also known as triflic acid, TFMS, TFSA, HOTf or TfOH, is a sulfonic acid with the chemical formula CF3SO3H. It is one of the strongest acids. Triflic acid is mainly used in research as a catalyst for esterification. It is a hygroscopic, colorless, slightly viscous liquid which is soluble in polar solvents.
==Synthesis==
Trifluoromethanesulfonic acid is produced industrially by electrochemical fluorination (ECF) of methanesulfonic acid:
:CH3SO3H + 4 HF → CF3SO2F + H2O + 1.5 H2
The resulting CF3SO2F is hydrolyzed, and the resulting triflate salt is preprotonated. Alternatively, trifluoromethanesulfonic acid arises by oxidation of trifluoromethylsulfenyl chloride:
::CF3SCl + 2 Cl2 + 2 H2O → CF3SO2OH + 4 HCl
Triflic acid is purified by distillation from triflic anhydride.〔

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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