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Ethyl diethoxyacetate

Anhydrous dimethylamine may be conveniently prepared by allowing 25% aqueous dimethylamine to drop onto solid potassium hydroxide, the gas evolved being dried by passage over solid potassium hydroxide. [Pg.59]

The compound is hygroscopic, and care should be taken to prevent exposure to air. [Pg.59]

Similar procedures for this preparation have been reported by Brown and Short3 and by Copenhaver and Kleinschmidt.4 [Pg.59]

1 Department of Chemistry, Polytechnic Institute of Brooklyn, Brooklyn 2, New York. [Pg.59]

ETHYL DIETHOXYACETATE (Glyoxylic acid, ethyl ester, diethyl acetal) [Pg.59]


Acid moieties include formic acid itself, formates and orthoesters, formamide, DMF dimethyl acetal and ethyl diethoxyacetate, acids, acid chlorides and anhydrides, the last including a rare [3,4-oxalate esters, 2-acyl or 2-ethoxycar-bonyl derivatives e.g. 180) are formed. [Pg.223]

Ethyl diazoacetate, 36, 25 Ethyl dichloroacetate, 32, 47 Ethyl diethoxyacetate, 35, 59 Ethyl enanthylsuccinate, 34, 51 Ethylene, 32, 100 37, 65 Ethylene, 1,1-dichloro-2,2-dipi.uoro-,... [Pg.49]

Ethyl diethoxyacetate has been prepared from dichloroacetic acid by the action of sodium ethoxide followed by esterification of the intermediate diethoxyacetic acid. This esterification has been carried out with ethyl iodide on the sodium salt or on the silver salt.5 6 7 It has been more conveniently done with ethanol and acid.8 910 Poorer yields are reported when the dichloroacetic acid is first esterified and then treated with sodium ethoxide.11... [Pg.62]

Preparation. The reagent (1) is prepared in 70% yield by the reaction of ethyl diethoxyacetate with 1,3-propanedithiol in the presence of boron trifluoride etherate. [Pg.230]

C8H160 3-ethyl-3-methyl-2-pentanone 19780-65-5 426.60 35.570 1,2 15233 C8H1604 ethyl diethoxyacetate 6065-82-3 472.15 41.215 1,2... [Pg.474]

Ethyl diazoacetate, 228-230,325 Ethyl diethoxyacetate, 230 Ethyldiisopropylamine, 230,368 Ethyl (3,0-dimethylacrylate, 249 l-Ethyl-3-(3 -dunethylaminopropyl)carbo-diimide hydrochloride, 26 Ethyl l,3-dithiane-2-carboxylate, 230-231 Ethylene, 11 Ethylene carbonate, 41 Ethylenediamine, 231,488 Ethylenediaminetetraacetic acid, 204 Ethylenediaminetetraacetic add disodium salt, 321... [Pg.324]

The reaction of dichloroacetic acid with ethanolic sodium ethoxide (a Williamson synthesis), followed by Fischer esterification, affords ethyl diethoxyacetate. The... [Pg.539]

CONJUGATE ADDITIONS Bis(methylthio)(trimethylsilyl)methyllithium. Diethylalum-inum cyanide. Di(a-methoxyvinyl)copperlithium. Ethyl diethoxyacetate. Ethyl methylsulfinylacetate. Lithium a-carboethoxy vinyl(l-hexynyl)cuprate. Potassium fluoride. Quinine, chinchonine. Titanium tetrachloride. Trimethylaluminum. Tris-(phenylthio)methyllithium. [Pg.778]

Ethyl diethoxyacetate reacted with 2,3- and 3,4-DAP in the presence of sodium methylate at 120-140 °C to afford IPs 2-aldehyde acetals (yields 26 and 24%)... [Pg.167]

Related Reagents. Ethyl Diethoxyacetate Glyoxylic Acid Diethyl Dithioacetal Ketene Bis(trimethylsilyl) Acetal Ketene Diethyl Acetal l-Methoxy-2-trimethylsilyl-l-(trimethylsilyl-oxyjethylene Methyl Glyoxylate 8-Phenyhnenthyl Glyoxylate Tetramethoxyethylene Tris(trimethylsilyloxy)ethylene. [Pg.236]


See other pages where Ethyl diethoxyacetate is mentioned: [Pg.59]    [Pg.61]    [Pg.61]    [Pg.349]    [Pg.712]    [Pg.94]    [Pg.95]    [Pg.95]    [Pg.349]    [Pg.253]    [Pg.364]    [Pg.365]    [Pg.356]    [Pg.357]    [Pg.514]    [Pg.304]    [Pg.732]    [Pg.167]    [Pg.359]    [Pg.343]    [Pg.344]    [Pg.397]   
See also in sourсe #XX -- [ Pg.35 , Pg.59 ]

See also in sourсe #XX -- [ Pg.35 , Pg.59 ]

See also in sourсe #XX -- [ Pg.35 , Pg.59 ]

See also in sourсe #XX -- [ Pg.230 ]

See also in sourсe #XX -- [ Pg.35 , Pg.59 ]

See also in sourсe #XX -- [ Pg.35 , Pg.59 ]

See also in sourсe #XX -- [ Pg.253 ]

See also in sourсe #XX -- [ Pg.253 ]

See also in sourсe #XX -- [ Pg.35 , Pg.59 ]




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