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Methyl pentafluoroethyl

Methyl Pentafluoroethyl Tellurium4 A mixture of 9.0 g (57.1 mmol) dimethyl tellurium and 17.9 g... [Pg.440]

Methyl Pentafluoroethyl Tellurium A mixture of 9.0 g (57.1 mmol) dimethyl tellurium and 17.9 g (72.8 mmol) pentafluoroethyl iodide is treated with 2.3 g (22.8 mmol) triethylamine at — 78° in a flask equipped with a low-temperature reflux condenser. The mixture is allowed to warm to 20 and then irradiated for 3 h with the reflux condenser kept at — 35°. The mixture is fractionally distilled to give methyl pentafluoroethyl tellurium as a light-yellow liquid that is stable toward water but easily oxidized yield 63% b.p. 42°. [Pg.440]

Fluorination. Fluorination of unsaturated compounds with CoF, is carried out in a stainless steel vessel from -196° to room temperature. The method transforms methyl trifluorovinyl ether to methyl pentafluoroethyl ether in 70% yield. [Pg.142]

Methyl pentafluoroethyl ether FIFE-254cb2 CH3OCF3CHF3 2.6 0.28 1260 359 109... [Pg.2299]


See other pages where Methyl pentafluoroethyl is mentioned: [Pg.545]    [Pg.545]    [Pg.440]    [Pg.545]    [Pg.164]    [Pg.486]    [Pg.487]    [Pg.969]    [Pg.1052]    [Pg.478]    [Pg.479]    [Pg.955]    [Pg.1036]    [Pg.1028]    [Pg.1117]    [Pg.465]    [Pg.466]    [Pg.919]    [Pg.998]    [Pg.527]    [Pg.528]    [Pg.1160]    [Pg.1259]    [Pg.2440]    [Pg.522]    [Pg.1041]    [Pg.1132]    [Pg.515]    [Pg.516]    [Pg.1161]    [Pg.1275]    [Pg.526]    [Pg.527]    [Pg.1157]    [Pg.1256]    [Pg.2511]    [Pg.478]    [Pg.479]    [Pg.953]    [Pg.1032]    [Pg.2249]   
See also in sourсe #XX -- [ Pg.440 , Pg.441 ]

See also in sourсe #XX -- [ Pg.440 , Pg.441 ]




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Pentafluoroethyl

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