Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Acetyl chloride | HCID 6367 | — |
| Edukt | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2,2,2-Trifluoroethyl Acetate | HCID 136256 | 72,9% |
Reaktionsschritte
85 g (0.85 mol) of trifluoroethanol and 80 ml of diethyl ether were poured to a four-neck flask of 2 liter, and further 129 g (1.27 mmol/1.49 eq) of triethylamine was added thereto. Then, the resultant mixture was ice-cooled and stirred while dropping a solution diluting 100 g (1.27 mol/1.49 eq) of acetyl chloride with 80 ml of diethyl ether by dropping funnel. While dropping, the temperature of the resultant reacted solution was kept between 27 to 35° C. The period of time for dropping was 20 minutes. After that, the resultant mixed solution was stirred for 1.5 hours at room temperature and 350 ml of water was added, then, the reaction was completed. Subsequently, an organic phase was separated by the separatory funnel and dried using magnesium sulfate. Thereafter, purification by distilling was conducted to obtain 88 g of 2,2,2-trifluoroethyl acetate (CH3COOCH2CF3) of which yield was 72.9%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08097368B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-8f312fc7dd90401daed4df06ef8cc951 |
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| Quellennotiz | uspto-grants-2012_01 |
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