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Furan 2,5-dihydroxymethyl

Furandicarboxylic acid Fructose, glucose (via HMF intermediate) Diol, amine, levulinic acid, succinic acid, 2,5 -fu rand icarbaldehyde, 2,5-dihydroxymethyl-furan, tetrahydrofuran, polyethylene, terephthalate analogues. Werpy and Petersen 2004... [Pg.88]

Thiophene derivatives were also prepared from the respective furans 2 [37]. Thus, the 2,5-dihydroxymethyl thiophenes were obtained from 2 by reduction, protection of the hydroxyl groups, oxidation with m-chloroperbenzoic acid to the respective cis-hexenedione whose reduction with titanium trichloride and subsequent reaction with Lawesson reagent gave the protected thiophene derivative. [Pg.5]


See other pages where Furan 2,5-dihydroxymethyl is mentioned: [Pg.23]    [Pg.23]    [Pg.42]    [Pg.23]    [Pg.23]    [Pg.199]    [Pg.199]    [Pg.23]    [Pg.23]    [Pg.199]    [Pg.23]    [Pg.23]    [Pg.199]   
See also in sourсe #XX -- [ Pg.101 ]




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