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2.2- difluoro-3-methylbutane

The products of the selective electrochemical fluorination of butadiene with platinum electrodes in amine/ HF mixtures, particularly Et,N 3HF, were 3,4-difluorobut-1-cnc and 1,4-difluorobut-2-ene in a ratio of 1 2, 2.3-dimethyIbut-2-enc gave 2.3-difluoro-2,3-dimelhylbutane (yield 22%), while 2-mcthylbut-2-ene gave 2,3-difluoro-2-methyIbutanc (yield 23%) and 2,2-difluoro-3-methylbutane (yield 11 %). Oct-1-ene could not be fluorinated instead, the solvent degraded. Volatile degradation products were acetaldehyde, acetyl fluoride and fluorocthane. [Pg.309]

Trimethylacetaldehyde reacts with sulfur tetrafluoride with a skeletal rearrangement 2,3-difluoro-2-methylbutane is formed in high yield as the only fluo-roalkane along with bis(l-fluoro-2,2-dimethylpropyl) ether [169] (equation 85)... [Pg.237]

C5H10F2 1,3-difluoro-2-methylbutane 66688-43-5 179.91 7.820 2 5652 C5H11F 1 -fluoro-2-methyl butane 10086-64-3 162.76 8.263 2... [Pg.560]

See other pages where 2.2- difluoro-3-methylbutane is mentioned: [Pg.122]    [Pg.431]    [Pg.605]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.122]    [Pg.122]    [Pg.122]    [Pg.122]    [Pg.122]    [Pg.122]    [Pg.122]    [Pg.122]    [Pg.325]    [Pg.325]    [Pg.325]    [Pg.325]    [Pg.325]    [Pg.431]    [Pg.431]    [Pg.431]    [Pg.431]    [Pg.431]    [Pg.431]    [Pg.431]    [Pg.431]    [Pg.431]    [Pg.431]    [Pg.560]    [Pg.560]    [Pg.560]    [Pg.560]    [Pg.560]    [Pg.560]    [Pg.605]    [Pg.605]    [Pg.605]    [Pg.605]    [Pg.605]    [Pg.605]    [Pg.702]   
See also in sourсe #XX -- [ Pg.107 ]

See also in sourсe #XX -- [ Pg.179 ]



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2 Methylbutane

2- Methylbutan

3- methylbutanal

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