トリエトキシ(1H,1H,2H,2H-ノナフルオロヘキシル)シラン

Nonafluorobutyl iodide (NFBI) and triethoxyvinylsilane (TEOVS) were fed into a three-necked flask equipped with a reflux condenser at a molar ratio of 1: 1.1 and then heated to 60 ℃ with stirring. When the internal temperature of the flask was sufficiently heated, azobisbutylnitrile (AIBN), a thermal decomposition radical initiator, was dissolved in an ether-based solvent. Then 0.5 ml/sec was dropped slowly into the stirred flask. After that, when the dropwise addition was completed, the external heating temperature was again set to 60 ℃ and stirred for 6 hours. After that, the internal temperature of the flask was lowered to room temperature (25 ℃), and tributyltin hydride (TBTH) was added to the flask at a rate of 1 ml/sec. After further stirring for 4 hours, distillation under reduced pressure at 1 Torr and 40 ° C yielded Nonafluorohexyltriethoxysilane (1H,1H,2H,2H-Perfluorohexyltriethoxysilane) in 75% yield.