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Potassium nitrosodisulfonate, reaction with phenols

Uncondensed phenolic units in lignin have been estimated by a color reaction based on oxidation with potassium nitrosodisulfonate (Fremy s salt) (Adler and Lundquist 1961) as illustrated below ... [Pg.28]

Ellipticine (E) 1 is an indolic alkaloid with antitumor activity. Some of its phenolic derivatives as N-methyl-9-hydroxyellipticine (Celiptinium), obtained from 9-hydroxy ellipticine (9-OH E), exhibit high cytotoxicity. 38 Syntheses of 9-OH E are not satisfactory considering yields and cost, justifying the attempts at the direct conversion of E to 9-OH E via 9-oxoellipticine (9-0X0 E). Potassium nitrosodisulfonate (Fremy s salt), a valuable oxidant for the synthesis of quinone-imine from heterocyclic amines,139 was used. Under these conditions the conversion of E to 9-0X0 E was observed for the first time. Its reduction to 9-OH E is then easily achieved with ascorbic acid. The radical nature of Fremy s salt [ 0-N(S03K)2] led us to carry out the oxidation reaction under sonication in order to increase the yields via an easier electron transfer.1 1... [Pg.374]

Phenols are aromatic counterparts of alcohols but are much more acidic (pkia 10) because their anions are resonance stabilized by delocalization of the negative charge into the aromatic ring. Phenols can he oxidized to quinones by reaction with Fremy s salt (potassium nitrosodisulfonate), and quinones can he reduced to hydroquinones by reaction with NaBH4. [Pg.539]

The nitrosodisulfonate salts, particularly the dipotassium salt called Fremy s salt, are useful reagents for the selective oxidation of phenols and aromatic amines to quinones (the Teuber reaction). - Dipotassium nitrosodisulfonate has been prepared by the oxidation of a hydroxylaminedisulfonate salt with potassium permanganate, " with lead dioxide, or by electrolysis. This salt is also available commercially. The present procedure illustrates the electrolytic oxidation to form an alkaline aqueous solution of the relatively soluble disodium nitrosodisulfonate. This procedure avoids a preliminary filtration which is required to remove manganese dioxide formed when potassium permanganate is used as the oxidant. " ... [Pg.124]


See other pages where Potassium nitrosodisulfonate, reaction with phenols is mentioned: [Pg.631]    [Pg.631]    [Pg.687]    [Pg.695]    [Pg.707]    [Pg.715]    [Pg.631]    [Pg.687]    [Pg.695]    [Pg.138]   
See also in sourсe #XX -- [ Pg.631 ]

See also in sourсe #XX -- [ Pg.631 ]

See also in sourсe #XX -- [ Pg.653 ]




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Phenol phenolation reaction

Phenol reactions

Phenolates, reactions

Phenolation reaction

Phenols potassium nitrosodisulfonate

Phenols reactions with

Potassium nitrosodisulfonate

Potassium phenolate

Potassium reactions

Potassium, reaction with

Reaction with phenolates

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