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Ethyl hydracrylate

It is important to carry out the esterification as rapidly as possible in order to cut down to a minimum the formation of ethyl hydracrylate, which takes place by the action of water on the (3-bromopropionic acid or ester an efficient condenser is therefore necessary. For the same reason it is necessary to remove all residual water from the mixture before adding the alcohol. [Pg.52]

Ethyl bromide, I, i, 6-7 Ethyl 8-bromopropionate, HI, 51-52 Ethyl cyanoacetate. III, 53-56 Ethylene chlorohydrin, 111, 7 Ethyl ether. III, 47, 48 Ethyl hydracrylate. III, 52 Ethyl oxalate, II, 23-26 Ethyl phenylacetate, II, 27-28 Extraction, III, 88... [Pg.52]

ETHYL P-HYDROXY-P.P-DIPHENYLPROPIONATE (Hydracrylic acid, 3,3-diphenyl, ethyl ester)... [Pg.56]

See other pages where Ethyl hydracrylate is mentioned: [Pg.134]    [Pg.52]    [Pg.173]    [Pg.27]    [Pg.68]    [Pg.51]    [Pg.173]    [Pg.173]    [Pg.134]    [Pg.52]    [Pg.173]    [Pg.27]    [Pg.68]    [Pg.51]    [Pg.173]    [Pg.173]    [Pg.29]    [Pg.912]    [Pg.217]    [Pg.14]    [Pg.797]    [Pg.916]   
See also in sourсe #XX -- [ Pg.3 , Pg.52 ]

See also in sourсe #XX -- [ Pg.3 , Pg.52 ]

See also in sourсe #XX -- [ Pg.3 , Pg.52 ]

See also in sourсe #XX -- [ Pg.3 , Pg.52 ]



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Ethyl hydracrylate, III

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