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Sodium 1-naphthalenesulfonate, formation

Of-Naphthoic acid has been prepared by the hydrolysis of a-naphthyl cyanide and (in poor yield) by the fusion of sodium a-naphthalenesulfonate and sodium formate. It has also been prepared by passing carbamyl chloride into naphthalene and aluminum chloride and hydrolyzing the a-napthamide thus formed.3... [Pg.83]

Meinwald et al. (76JA6643) described reactions with sodium hydroxide and lithium phenylamide leading to the formation of sodium 1-naphthalenesulfonate (69) and 1-naphthalenesulfonamide (70), respectively. Again, the negatively charged fragment of the reagent attacks the sulfur atom, followed by protonation of the atom of the naphthalene core (Scheme 13). [Pg.17]


See other pages where Sodium 1-naphthalenesulfonate, formation is mentioned: [Pg.166]    [Pg.31]    [Pg.31]    [Pg.83]    [Pg.363]    [Pg.364]    [Pg.99]    [Pg.25]    [Pg.502]   
See also in sourсe #XX -- [ Pg.17 ]




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