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Cetylmalonic ester

Catalyst, alumina, 34, 79 35, 73 ammonium acetate, 31, 25, 27 copper chromite, 31, 32 36, 12 cuprous oxide-silver oxide, 36, 36, 37 ferric nitrate, hydrated, 31, 53 piperidine, 31, 35 piperidine acetate, 31, 57 Raney nickel, 36, 21 sulfuric acid, 34, 26 Catechol, 33, 74 Cetylmalonic acid, 34, 16 Cetylmalonic ester, 34,13 Chlorination, by sulfuryl chloride, 33, 45 ... [Pg.46]

CETYLMALONIC ESTER (Malonic acid, cetyl-f diethyl ester)... [Pg.13]

The residual a-ethoxalyl ester is decarbonylated to cetyl-malonic ester by heating at 160-170° under reduced pressure. A water aspirator is sufficient to facilitate removal of the carbon monoxide formed during the heating. The decarbonylation requires about 1-1,5 hours (Note 7). The cetylmalonic ester which remains as a dark liquid is fractionated under reduced pressure (Note 8). [Pg.14]

This method is based on the general procedure previously described by Floyd and Miller.2 Cetylmalonic ester has also been prepared by condensation of ethyl stearate with ethyl carbonate 8 and by alkylation of sodiomalonic ester with cetyl iodide4 or cetyl bromide.8... [Pg.16]

Cetylmalonic acid, m.p. 115.5-120.5°, is obtained by saponification of the ester and one crystallization from acetone. [Pg.16]


See other pages where Cetylmalonic ester is mentioned: [Pg.13]    [Pg.15]    [Pg.232]    [Pg.70]    [Pg.71]    [Pg.13]    [Pg.15]    [Pg.232]    [Pg.70]    [Pg.71]   
See also in sourсe #XX -- [ Pg.13 , Pg.34 ]

See also in sourсe #XX -- [ Pg.13 , Pg.34 ]

See also in sourсe #XX -- [ Pg.13 , Pg.34 ]

See also in sourсe #XX -- [ Pg.13 , Pg.34 ]

See also in sourсe #XX -- [ Pg.13 , Pg.34 ]

See also in sourсe #XX -- [ Pg.13 , Pg.34 ]

See also in sourсe #XX -- [ Pg.13 , Pg.34 ]




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