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N-Butylglycidyl ether

Then, 52.0 g (0.4 mol) n-butylglycidyl ether and 41A g (0.44 mol) phenol was added thereto, whereafter the material was heated to boiling under nitrogen. The material was stirred, about 8.5 hours, until no glycidyl ether could be determined, e.g., by gas chromatography. [Pg.619]

For example, the phosgenation of n-butylglycidyl ether in toluene, in presence of 0.5 mol.% HBGCI, at 30°C within 2 h, gave the corresponding 1-chloromethyl-2-n.butoxy ethyl chloroformate in 96% yield. This chloroformate is the key starting material for the preparation of an intermediate carbamate used in the Febarbamate manufacture as shown in scheme 55. [Pg.29]

N-BUTYLGLYCIDYL ETHER CJLOCH.CHOCH, BGE 1,2 Epoxy-3>butoxy-propane Strong oxidizers and caustics 130 ... [Pg.216]

See other pages where N-Butylglycidyl ether is mentioned: [Pg.619]    [Pg.1619]    [Pg.1554]    [Pg.619]    [Pg.1619]    [Pg.1619]    [Pg.619]    [Pg.1619]    [Pg.1554]    [Pg.619]    [Pg.1619]    [Pg.1619]    [Pg.1521]    [Pg.4263]    [Pg.4262]   


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