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Sodium acetamide phenolate

Chloroethyl vinyl ether, 2-Chlorophenol, Cyclohexene, Dalapon-sodium. Diallate. 1,1-Dichloroethane, 2,3-Dimethylamine, Dimethylbutane, 1,4-Dioxane, Ethylamine, Ethyl ether, Erhvl sulfide. 2-Heptanone, Metaldehvde. 2-Methvlbutane. 2-Methvl-2-butene. 2-Methyl phenol, Nitromethane, 4-Nitrophenol, 2-Nitropropane, 1-Octene, 2-Pentanone, Phenol, Toluene, Triethylamine, Vinyl chloride, o-Xylene, m-Xylene Acetamide, see Acetonitrile, Acrylamide, Acrylonitrile, Ethylamine... [Pg.1518]

Perfluoro[AT-fluoro-Af-(4-pyridyl)acetamide], prepared via direct fluorination of the sodium salt of perfluoro[/V-(4-pyridyl)acetamide], readily fluorinates diethyl sodio(phenyl)malonate, 1-morpholinocyclohexene, phenol and anisole under mild conditions.129... [Pg.472]

The gas-phase equilibrium between 2-hydroxypyridine and 2-pyridone favours the hydroxy-form, but in the equilibrium between 2-hydroxypyridine iV-oxide and N-hydroxy-2-pyridone, the major tautomer is the hydroxy-pyridone. Bicyclic adducts between 2-pyridones and dimethyl acetylene-dicarboxylate, unobtainable at atmospheric pressure, have been obtained at 10—15 kbar. A novel route to iV-hydroxy-2-pyridone involves the trimethyl-silylation of 2-pyridone followed by oxidation of the resulting 2-(trimethyl-silyloxy)pyridine with the DMF complex of molybdenum pentoxide. p-Nitro-phenols (45) and nitro-acetamides (46) are formed from the reaction of 3,5-dinitro-2-pyridones (43) with the sodium salts of /3-keto-esters (44) (Scheme 20). ... [Pg.231]

Dimethyl sulfoxide is generally favored, particularly with processes using sodium hydroxide as base. In carbonate polymerizations, the presence of free phenolic hydroxyl groups at polymerization temperatures of 150-160°C leads to undesirable side reactions Involving acid catalyzed decomposition of OMSO which ultimately can lead to stoichiometry upsets. For polymerizations involving carbonate, dimethyl acetamide is often the solvent of choice [7], DMSO is limited by its 180 C boiling point to temperatures of 170 C or lower while DMAc is useful in the 150-160 C range. [Pg.155]


See other pages where Sodium acetamide phenolate is mentioned: [Pg.331]    [Pg.398]    [Pg.331]    [Pg.398]    [Pg.178]    [Pg.325]    [Pg.244]    [Pg.262]    [Pg.627]    [Pg.274]   
See also in sourсe #XX -- [ Pg.717 ]




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