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Acetic acid, cyanoesters

A variety of other carbon nucleophiles have been alkylated with alcohols including malonate esters, nitroaUcanes, ketonitriles [119, 120], barbituric acid [121], cyanoesters [122], arylacetonitriles [123], 4-hydroxycoumarins [124], oxi-ndoles [125], methylpyrimidines [126], indoles [127], and esters [128]. Selected examples are given in Scheme 35. Thus, benzyl alcohol 15 could be alkylated with nitroethane 147, 1,3-dimethylbarbituric acid 148, phenylacetonitrile 149, methyl-pyrimidine 150, and even f-butyl acetate 151 to give the corresponding alkylated products 152-156. [Pg.102]


See other pages where Acetic acid, cyanoesters is mentioned: [Pg.244]    [Pg.263]    [Pg.415]    [Pg.936]    [Pg.669]   


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Acetic acid, cyanoesters Vilsmeier-Haack reaction

Cyanoester

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