反応 #1755449

反応方程式

potassium hydroxide

2,2,3,3,4,4,4-heptafluorobutan-1-ol

1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride

potassium hydroxide

→

crude product

収率 72.6%

2,2,3,3,4,4,4-heptafluorobutyl 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate

収率 72.6%

反応条件

後処理

1. 1
   その他The flask was equipped with an overhead mechanical stirrer, cold water condenser
2. 2
   その他did not exceed 35° C
3. 3
   ろ過Precipitated salts were then filtered from the mixture
4. 4
   その他the lower liquid fluorochemical product phase was separated from the upper aqueous phase
5. 5
   洗浄washed once with water

実験手順

2,2,3,3,4,4,4-heptafluorobutan-1-ol (200 g, 1.0 mol, obtained from 3M Company) and 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonyl fluoride (300 g, 1.0 mol, obtained from 3M Company) were combined in a 1-liter, 3-necked round bottom flask. The flask was equipped with an overhead mechanical stirrer, cold water condenser, thermocouple and an addition funnel. Aqueous potassium hydroxide (45 percent by weight in water, 154 g, 1.05 mol) was added dropwise via the addition funnel at such a rate that the temperature did not exceed 35° C. Once the addition of the potassium hydroxide was complete, the mixture was stirred for 16 hours at room temperature. Precipitated salts were then filtered from the mixture and the lower liquid fluorochemical product phase was separated from the upper aqueous phase and washed once with water to give 350 g crude product. The product was distilled at atmospheric pressure and the distillation cut boiling from 140-150° C. used without further purification (96.3 percent purity by GC).

出典