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Ethyl 2-furoate

Ethyl furoate (2-Furancarboxylic acid, ethyl ester) COOC2H5... [Pg.192]

Ethyl furoate undergoes a Friede 1-Crafts condensation with tertiary chlorides in carbon disulfide solution. The free alkylfuroic acids are oxidized by alkaline potassium permanganate to trialkylacetic acids. Dimethylethylacetic acid (65%) and 1-methyl-l-cyclohexylcarboxylic acid (44%) have been prepared in this manner. ... [Pg.216]

Fur furol 2-Ethyl furoate 2-Me thoxyf Liran Dibenzofuran 3-Furoic acid ... [Pg.259]

Benzoic acid 85 Citronellyl isobutyrate 133 Ethyl furoate... [Pg.1056]

Products and Uses There are 4000 ingredients in cigarettes. Additives include yeast, wine, caffeine, beeswax, and chocolate. Other ingredients, or by-products, include ammonia, angelica extract (which is a carcinogen in animals), benzene, benzopyrene, butone, cadmium, cyanide, DDT, ethyl furoate, lead formaldehyde, methoprene (insecticide), napthalene, and tars, and so on. [Pg.91]

A variety of 2-substituted-3-pyridinols can be prepared by well-known methods. For example, diarylmethyl 2-lliryl ketones are prepared in good yield from ethyl fliroate and diarylmethanes using KNH2 or NaNHj in liquid ammonia and are conveniently converted to XII-279. p-Chlorobenzyl 2-furyl ketones, which can be converted to XU-280, can be prepared from p-chlorophenylacetonitrile and ethyl furoate by condensation in the presence of alkoxide followed by hydrolysis and decarboxylation. 2-Pyrryl ketones are also formed in the last step. Several 2-furyl ketones are cleaved under these reaction conditions and do not give 3-pyridinols. ... [Pg.667]


See other pages where Ethyl 2-furoate is mentioned: [Pg.628]    [Pg.628]    [Pg.398]    [Pg.94]    [Pg.1355]    [Pg.1355]    [Pg.628]    [Pg.628]    [Pg.628]    [Pg.628]    [Pg.533]    [Pg.364]    [Pg.314]    [Pg.398]    [Pg.313]    [Pg.299]    [Pg.98]    [Pg.116]    [Pg.179]    [Pg.99]    [Pg.372]   
See also in sourсe #XX -- [ Pg.91 ]




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