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Grignard reaction with methyl sulfate

Lithiation of dibenzofuran with butyllithium and mercuration both occur at the 4-position. Thallation occurs at the 2-position, however (57IZV1391). The mercury and thallium derivatives serve as a source of the iodo compounds by reaction with iodine. Bromodibenzofurans undergo bromine/lithium exchange with butyllithium and the derived lithio compounds may be converted into phenols by reaction with molecular oxygen in the presence of a Grignard reagent, into amines by reaction with O-methylhydroxylamine, into sulfinic acids by reaction with sulfur dioxide, into carboxylic acids by reaction with carbon dioxide and into methyl derivatives by reaction with methyl sulfate (Scheme 100). This last reaction... [Pg.643]


See other pages where Grignard reaction with methyl sulfate is mentioned: [Pg.439]    [Pg.167]    [Pg.240]    [Pg.244]    [Pg.826]    [Pg.293]    [Pg.118]    [Pg.186]    [Pg.875]    [Pg.875]    [Pg.826]    [Pg.158]    [Pg.289]    [Pg.44]    [Pg.230]    [Pg.382]    [Pg.974]    [Pg.1313]    [Pg.1116]    [Pg.2227]    [Pg.2886]    [Pg.117]    [Pg.83]    [Pg.187]    [Pg.35]    [Pg.742]    [Pg.179]    [Pg.947]    [Pg.382]    [Pg.974]    [Pg.1313]    [Pg.382]    [Pg.974]    [Pg.1313]   
See also in sourсe #XX -- [ Pg.11 , Pg.66 ]

See also in sourсe #XX -- [ Pg.11 , Pg.66 ]




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Methyl Grignard

Methyl sulfate

Methyl sulfate, reactions

Sulfate reaction

Sulfation reaction

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