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3.5- Dibromo-4-methylacetophenone

Terephthalic acid has been obtained from a great many /)-disubstituted derivatives of benzene or cyclohexane by oxidation with permanganate, chromic acid, or nitric acid. The following routes appear to have preparative value from />-toluic acid, />-methylacetophenone,2 or dihydro-/)-tolualdehyde by oxidation with permanganate from f>-cymene by oxidation with sodium dichromate and sulfuric acid from />-dibromobenzene or from /i-chloro- or -bromobenzoic acid by heating at 250° with potassium and cuprous cyanides and from />-dibromo-benzene, butyllithium, and carbon dioxide. ... [Pg.96]

See other pages where 3.5- Dibromo-4-methylacetophenone is mentioned: [Pg.111]    [Pg.56]    [Pg.113]    [Pg.56]    [Pg.9]    [Pg.111]    [Pg.56]    [Pg.113]    [Pg.56]    [Pg.66]   
See also in sourсe #XX -- [ Pg.9 , Pg.40 ]

See also in sourсe #XX -- [ Pg.9 , Pg.40 ]

See also in sourсe #XX -- [ Pg.9 , Pg.40 ]

See also in sourсe #XX -- [ Pg.9 , Pg.40 ]



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4-Methylacetophenone

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