反应 #1755447
ord-6dbc69d7de7642a3b9a628ff52f0a4f2
反应方程式
反应物
试剂
溶剂
反应条件
后处理
- 1其他The flask was equipped with a magnetic stirrer, cold water condenser
- 2workup.ADDITIONthermocouple and a 250-mL addition funnel
- 3其他did not exceed 35° C
- 4workup.ADDITIONOnce the addition of the base
- 5过滤The precipitated salts were then filtered from the mixture
- 6其他the lower liquid fluorochemical product phase was separated from the upper aqueous phase
- 7其他were removed by atmospheric distillation
实验过程
2,2,3,4,4,4-hexafluorobutan-1-ol (202 g, 1.1 mol, obtained from Sinochem Corp., Beijing, China), 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride (332 g, 1.1 mol, obtained from 3M Company of Saint Paul, Minn.) and water (300 g) were combined in a 3-L, 3-necked round bottom flask. The flask was equipped with a magnetic stirrer, cold water condenser, thermocouple and a 250-mL addition funnel. Aqueous potassium hydroxide (149.3 g, 45 weight percent, 1.22 equivalents) was added dropwise via an addition funnel at such a rate that the temperature did not exceed 35° C. Once the addition of the base was complete the mixture was stirred for 16 hours at room temperature. The precipitated salts were then filtered from the mixture and the lower liquid fluorochemical product phase was separated from the upper aqueous phase. Unreacted 2,2,3,4,4,4-hexafluorobutan-1-ol and 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride were removed by atmospheric distillation.