The electrochemical fluorination of aliphatic primary monohydric alcohols and aldehydes.

スポンサーリンク

概要

• 論文の詳細を見る

• The perfluorocyclic ethers as well as the perfluoroalkanoyl fluorides were obtained by the electrochemical fluorination of primary monohydric alcohols and aldehydes containing 4–8 carbon atoms. The five-membered rather than the six-membered perfluorocyclic ethers were formed as the cyclic products. The over-all yields of the perfluorocyclic ethers and the perfluoroalkanoyl fluorides from the alcohols were in the range of 10–20%, and 3–12% respectively. Those from the aldehydes were poor because of the formation of a considerable amount of tarry by-products. The physical properties of the perfluorocyclic ethers obtained are also described.

• 公益社団法人 日本化学会の論文

著者

• Nagase Shunji

  Government Industrial Research Institute

• Baba Hajime

  Government Industrial Research Institute

• Abe Takashi

  Government Industrial Research Institute, Nagoya

• Abe Takashi

  Government Industrial Research Institute

関連論文

• Electrochemical Fluorination of 2,2,3,3-Tetrafluoro-1-propanol
• Electrochemical Fluorination of Aldehydes
• The electrochemical fluorination of trifluoromethyl-substituted benzenes.
• Electrochemical fluorination of ethanethiol.
• The Electrochemical Fluorination of Dithiols and Cyclic Sulfides
• The electrochemical fluorination of aliphatic primary monohydric alcohols and aldehydes.
• The Fluorination of Carbon Monoxide, Carbonyl Chloride, and Carbonyl Fluoride
• The Fluorination of Carbonyl Sulfide
• Electrochemical fluorination of thiols.
• Chlorofluorination of Carbon Disulfide and Sulfur
• The Electrochemical Fluorination of s-Triazines
• The Electrochemical Fluorination of Benzenes and Pyridines

もっと見る 閉じる

スポンサーリンク