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Butane 2,3-Butanediol esters

Application To produce 1,4 butanediol (BDO) from butane via maleic anhydride and hydrogen using ester hydrogenation. [Pg.43]

Erylus formosus [45], was also reported by Kulkami et al. [53]. As shown in Fig. (19), a common bifunctional nine-carbon aldehyde was used for both syntheses. Both syntheses started with the DHP monoprotection of 1,4-butanediol, followed by subsequent PCC oxidation to the corresponding aldehyde. Reaction of this butanal with (4-carboxybutyl)triphenylphosphonium bromide resulted in the corresponding THP protected olefinic acid that was further deprotected and esterified to the methyl ester. A second oxidization with PCC afforded the desired intermediate methyl 8-formyloct-5-enoate which secured the cis A5 double bond in the final targets, Fig. (19). The... [Pg.85]

Davy Process Technology, U K Butanediol, 1,4- Maleic anhydride and hydrogen Process produces 1,4 butanediol (BDO) from butane via maleic anhydride and hydrogen using ester hydrogenation 11 NA... [Pg.299]

Long-chain unsaturated o, ct>-dicarboxylic acid methyl esters and their epoxidized derivatives were polymerized with 1,3-propanediol or 1,4-butane-diol in the presence of lipase CA catalyst to produce reactive polyesters [112]. The molecular weight of the polymer from 1,4-butanediol was higher than that from 1,3-propanediol. All the resulting polymers had a melting point ranging from 23 to 75 °C. [Pg.150]


See other pages where Butane 2,3-Butanediol esters is mentioned: [Pg.304]    [Pg.157]    [Pg.11]    [Pg.304]    [Pg.860]    [Pg.157]    [Pg.39]    [Pg.11]    [Pg.124]    [Pg.122]    [Pg.122]    [Pg.132]    [Pg.108]   
See also in sourсe #XX -- [ Pg.11 , Pg.412 ]




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1 : 4-Butanediol

1,4-butanediole

Butanediols

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