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Methyl ethylacetoacetate

Methyl-2-cyclopenten-2-ol-1-one Methyidihydrojasmonate Methyl ethylacetoacetate Methyl euqenol Methylfurfural... [Pg.5323]

The mercaptals obtained by the acid catalyzed reaction of J3-ketoesters, e.g., ethyl acetoacetate, with methyl thioglycolate (73) undergo the Dieckmann cyclization with alcoholic potassium hydroxide at lower temperatures to give ethyl 3-hydroxy-5-methyl-2-thiophenecarboxylate (74) in 75% yield. ° Besides ethyl acetoacetate, ethyl a-ethylacetoacetate, ethyl benzoyl acetate, and ethyl cyclopentanonecarboxylate were also used in this reaction/ It is claimed that /8-diketones, hydroxy- or alkoxy-methyleneketones, or /8-ketoaldehyde acetals also can be used in this reaction. From acetylacetone and thioglycolic acid, 3,5-dimethyl-2-thiophenecarboxyl-ic acid is obtained. ... [Pg.30]

Various thiourea ligands have been used in the synthesis of mixed ligand complexes. A series of complexes [NiQ2L2] (HQ = ethylacetoacetate, L = thiourea, allyl-, benzoyl-, methyl-, diphenyl-thiourea) have been prepared. The complexes are all paramagnetic (/i = 3.02-3.27/iB) and have been assigned tra 5-octahedral structures.1014... [Pg.337]

None of the products formed in the reactions described above is considered to significantly change the reaction rates and product distributions by acting as a catalyst. However, Siskin et al. [106] reported that in the hydrolysis of methyl 1-naphthoate at 343 °C naphthalene was predominantly formed because the potential for autocatalysis arises. They concluded that decarboxylation of naphthoic acid, the main product at a lower temperature of 250 °C, led to the formation of naphthalene at 343 °C the reaction is catalyzed by the generated carbonic acid. In the hydrolysis of typical p-keto esters, ethylacetoacetate was completely converted to acetone, eAanol, and CO2 within 30 min at 250 °C. Under the same conditions, r-butyl acetate degraded into a bright red, insoluble mixture of unidentifled products resulting from polymerization of isobutylene [107]. [Pg.271]

It may be prepared by the eondensation of one mole each of phenyl-hydrazine and the lactim-form of ethylacetoacetate when 1-phenyl-3-methyl-pyrazolone is obtained by the elimination of a mole each of water and ethanol. The resulting product is subjected to methylation either with methyl iodide or dimethyl sulphate to yield phenazone. [Pg.288]

Resorcinol interacts with the enoZ-form of ethylacetoacetate in the presence of concentrated sulphuric acid to 3ueld 7-hydroxy-4-methyl coumarin with the elimination of one mole each of ethanol and water. [Pg.132]

Diacetatopalladium. See Palladium diacetate Diacetic ether. See Ethylacetoacetate Diacetin (INCI). See Glyceryl diacetate Diacetone. See Diacetone alcohol Diacetone acrylamide CAS 2873-97-4 EINECS/ELINCS 220-713-2 Synonyms Acrylamide, N-(1-1dimethyl-3-oxobutyl)- 4-Acrylamido-4-methyl-2-pentanone DAA Diallyl ester acetic acid N-(1,1-Dimethyl-3-oxobutyl) acrylamide N-(1,1-Dimethyl-3-oxobutyl)-2-propenamide N-(2-(2-Methyl-4-oxopentyl)) acrylamide N-(2-Methyl-4-oxo-2-pentyl) acrylamide 2-Propenamide, N-(1,1-dimethyl-3-oxobutyl)-Classification Acrylamide Empirical C9H15NO2... [Pg.1196]

Ethyl acetoacetate 3-ethylene acetal Ethylacetoacetate ethyleneglycol acetal Ethyl acetoacetate ethyleneglycol ketal. See Ethyl acetoacetate ethylene ketal Ethyl acetoacetate ethylene ketal CAS 6413-10-1 EINECS/ELINCS 229-114-0 Synonyms 1,3-Dioxolane-2-acetic acid, 2-methyl-, ethyl ester Ethyl acetoacetate 3-ethylene acetal Ethylacetoacetate ethyleneglycol acetal Ethyl acetoacetate ethyleneglycol ketal Ethyl 2-methyl-1,3-dioxolane-2-acetate... [Pg.1683]

Amino-6-nitrobenzothiazole 2-Aminothiazole Ethylacetoacetate Metanilic acid Methyl acetoacetate dye mfg., azo, printing inks 3,3 -Dichlorobenzidine dihydrochloride dye mfg., azo acetate 4-Chloro-o-toluidine hydrochloride dye mfg., azo cotton 4-Chloro-o-toluidine hydrochloride dye mfg., azo crayons 3,3 -Dichlorobenzidine dihydrochloride dye mfg., azo nylon 4-Chloro-o-toluidine hydrochloride... [Pg.5133]

Benzyl alcohol Propylene glycol dioctanoate solvent, fragrances cosmetics Isobutyl acetate Methyl acetoacetate solvent, fragrances personal care Ethylacetoacetate solvent, fuel additives PPG-2 methyl ether PPG-3 methyl ether solvent, fuel oils Monochlorotoluene solvent, fuels... [Pg.5697]

From the experimental results obtained three liquid-liquid systems have been selected to be included here aniline/water, ethylacetate/water and ethylacetoacetate/water. The selected surfactants are SDS (sodium dodecyl sulphate), which is anionic, DTAB (dodecyl tri-methyl ammonium bromide), which is cationic, and Atlas G1300 (polyoxyethylene triglyceride ester) which is non-ionic. [Pg.43]

See 1-Methyl-l-ethylacetoacetic Acid. l-Methyl- acetobut]rric Acid... [Pg.603]

Methyl-1-ethylacetoacetic Acid (1-Methyl-l-acetobutyric acid)... [Pg.685]

Hagemann s-ester a compound prepared by treating a mixture of formaldehyde and ethylacetoacetate with base and then with acid and heat, half-chair conformation the least stable conformation of cyclohexane, haloform reaction the reaction of a halogen and HO — with a methyl ketone, halogenation reaction with halogen (Br, Cl, Ij). [Pg.1312]

Methyl-l-butyn-3-ol reacts with diketene or with ethylacetoacetate as follows ... [Pg.226]


See other pages where Methyl ethylacetoacetate is mentioned: [Pg.688]    [Pg.688]    [Pg.688]    [Pg.1314]    [Pg.1314]    [Pg.688]    [Pg.688]    [Pg.2627]    [Pg.2627]    [Pg.6527]    [Pg.6955]    [Pg.7051]    [Pg.688]    [Pg.688]    [Pg.688]    [Pg.1314]    [Pg.1314]    [Pg.688]    [Pg.688]    [Pg.2627]    [Pg.2627]    [Pg.6527]    [Pg.6955]    [Pg.7051]    [Pg.978]    [Pg.472]    [Pg.473]    [Pg.653]    [Pg.464]    [Pg.465]    [Pg.5851]    [Pg.331]    [Pg.2627]    [Pg.5234]    [Pg.5398]    [Pg.5416]    [Pg.395]    [Pg.210]    [Pg.451]    [Pg.513]    [Pg.508]    [Pg.501]    [Pg.502]   
See also in sourсe #XX -- [ Pg.153 , Pg.257 ]

See also in sourсe #XX -- [ Pg.153 , Pg.257 ]




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Ethylacetoacetate

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