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2.4- Dinitrophenyl ethers, from phenols

Dissolve 1 g. (or 0 01 mol) of the phenol in a solution of 0-40 g. of sodium hydroxide in 5 ml. of water. Add the resulting solution to 2-Og. of 2 4-dinitrochlorobenzene dissolved in 30 ml. of 95 per cent, ethanol add more alcohol, if necessary, to effect solution. Heat the solution under reflux on a water bath until the colour (usually red) is discharged and a copious precipitate of sodium chloride appears (30-60 minutes). Dilute the reaction mixture with an equal volume of water, filter off the precipitated 2 4-dinitrophenyl ether, wash with water, and recrystallise from alcohol. [Pg.684]

If the other product from the hydrolysis is phenol, the procedures described in Section 5.1 are applied to the preparation of the derivatives, particularly those which permit a very sensitive analysis. Perfluorinated acyl derivatives and 2,4-dinitrophenyl-, 2,6-dinitro-4-trifluoromethylphenyl and pentafluorophenyl ethers are frequently used [482], when concentrations of 0.01—0.1 ppb of the insecticide in water can be determined. [Pg.179]


See other pages where 2.4- Dinitrophenyl ethers, from phenols is mentioned: [Pg.164]    [Pg.224]    [Pg.244]    [Pg.153]   
See also in sourсe #XX -- [ Pg.1250 ]

See also in sourсe #XX -- [ Pg.1250 ]




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Dinitrophenylation

Ethere from phenols

Ethers, dinitrophenyl

From ethers

From phenols

Phenolic ethers

Phenols dinitrophenyl ethers

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