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Glyceryl monoformate

CH2(0H)CH(0H)CH2(0H) + HCOOH reaches about 100°, losing carbon dioxide and giving glyceryl monoformate (B). On further heating, particularly if more oxalic acid is added, the mono formate is hydrolysed (the necessary water being provided both by the oxalic acid and by the first reaction), and consequently a distillate of aqueous formic acid is obtained. [Pg.113]

If the reaction mixture used in the above preparation of formic acid is heated to 190-200°, the glyceryl monoformate which has escaped hydrolysis undergoes decomposition, with the loss of carbon dioxide and water, and the... [Pg.114]

See other pages where Glyceryl monoformate is mentioned: [Pg.222]    [Pg.222]   
See also in sourсe #XX -- [ Pg.113 , Pg.114 ]

See also in sourсe #XX -- [ Pg.222 ]

See also in sourсe #XX -- [ Pg.223 ]



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