Reaktion #439270

Reaktionsgleichung

4-cyclohexanedimethanol vinyl ether

acetonitrile

chlorotrifluoroethylene

→

desired product

Ausbeute 58.0%

2-Chloro-1,1,2-trifluoro-1-{[4-(vinyloxymethyl)cyclohexyl]methoxy}propane

Ausbeute 58.0%

Lösungsmittel

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigepartially evacuated
2. 2
   Sonstigecondensed
3. 3
   TemperaturAfter this, the PARR® reactor was cooled to room temperature
4. 4
   Sonstigeseparated
5. 5
   Einengenwas concentrated under reduced pressure 0.05 mmHg) at 25-30° C.

Vorschrift

Into a 450 mL capacity PARR® reactor, 1,.4-cyclohexanedimethanol vinyl ether (50 g, 294 mmol), acetonitrile (100 mL), and Cs2CO3 (2 g, 6 mmol) were added. The PARR® reactor was cooled to ˜30° C., partially evacuated and chlorotrifluoroethylene (34 g, 294 mmol) was condensed and the resultant mixture was heated at ˜50-60° C with stirring for 3 hours. After this, the PARR® reactor was cooled to room temperature, vented in the fume hood and the reaction mixture was poured into ˜150 mL water and the lower layer containing the crude product separated, and was concentrated under reduced pressure 0.05 mmHg) at 25-30° C. to afford the desired product as a colorless viscous liquid (49 g, 58% yield) which is a mixture of cis/trans isomers in the ratio 73:18; refractive index of 1.415 at 23.7° C.; GC/MS (EI mode): m/z at 286 for M+; 19F and 1H NMR spectral data are consistent with the structure.

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