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CAS RN: 2923-18-4 | 產品號碼: T1336
Sodium Trifluoroacetate
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產品規格
| Appearance | White to Almost white powder to crystal |
| Purity(Nonaqueous Titration) | min. 98.0 % |
| Solubility in Water | very faint turbidity |
| Water | max. 2.0 % |
性質
| 熔點 | 207 °C(dec.) |
| 水溶性 | Soluble |
| Degree of solubility in water | 625 g/l 20 °C |
GHS
相關法規
| RTECS # | AK0250000 |
運輸資料
| HS編碼* | 2915.90-900 |
Application
Trifluoromethylation of Aromatic Halides
Typical Procedure (Entry 1):
A mixture of iodobenzene (5 mmol), sodium trifluoroacetate (20 mmol), and copper (I) iodide (10 mmol) in N-methylpyrrolidone (NMP) (40 mL) is heated under argon atmosphere. Evolution of CO2 begins at around 140 ℃. After 4 h stirring at 160 ℃, the resulting mixture is diluted with diethylether - hexane (1 : 1), filtrated through celite layer, washed with water (3 times), and dried over MgSO4. By means of GC measurement of the solution, the yield of (trifluoromethyl)benzene is determined as 72%.
A mixture of iodobenzene (5 mmol), sodium trifluoroacetate (20 mmol), and copper (I) iodide (10 mmol) in N-methylpyrrolidone (NMP) (40 mL) is heated under argon atmosphere. Evolution of CO2 begins at around 140 ℃. After 4 h stirring at 160 ℃, the resulting mixture is diluted with diethylether - hexane (1 : 1), filtrated through celite layer, washed with water (3 times), and dried over MgSO4. By means of GC measurement of the solution, the yield of (trifluoromethyl)benzene is determined as 72%.
References
- A convenient trifluoromethylation of aromatic halides with sodium trifluoroacetate
Application
Difluorocarbene Precursor
Reference
- Sodium Trifluoroacetate: an Efficient Difluorocarbene Precursor for Alkenes
考研文獻
文章/手冊
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