反应 #81697
ord-c651a9626b3742698ca1704d02ec5745
溶剂
反应条件
后处理
- 1其他Into a 1 l four-necked flask equipped with a stirrer, a reflux condenser, a dropping funnel
- 2温度The reactor was heated
- 3其他to 60° C
- 4workup.ADDITIONAfter completion of the dropwise addition
- 5温度heating
- 6温度refluxing
- 7workup.WAITwere continued for 8 hours
- 8workup.DISSOLUTIONto dissolve
- 9其他precipitated potassium iodide
- 10其他The crude reaction solution
- 11其他was separated into two layers
- 12洗涤the fluorocarbon layer (lower layer) was further washed with 300 g of water
- 13其他to recover a fluorocarbon
实验过程
Into a 1 l four-necked flask equipped with a stirrer, a reflux condenser, a dropping funnel and a thermometer, 250 cc of methanol and 3 g of tetrabutylphosphonium bromide and 74.3 g (1.1 mols) of 85% potassium hydroxide were charged. The reactor was heated to bring the internal temperature to 60° C. Then, 273 g (0.5 mol) of C8F17I was dropwise added thereto over a period of one hour. After completion of the dropwise addition, heating and refluxing were continued for 8 hours. The conversion at that time was 99.6%. The reactor was cooled to room temperature. Then, 300 g of water was added to dissolve precipitated potassium iodide. The crude reaction solution was separated into two layers, and the fluorocarbon layer (lower layer) was further washed with 300 g of water to recover a fluorocarbon. Thus, 197 g of C8F17H having a purity of 99.0%, was obtained.