Process for producing glycoside
AssigneeMitsui Chemicals, Inc.
InventorsMasayuki Furuya, Hidetoshi Tsunoda, Tsuneji Suzuki, Akinori Nagatomo, Masaru Wada
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Abstract
A glycoside in which at least two phenolic hydroxyl groups of a compound having at least two phenolic hydroxyl groups in its molecule are glycosidically linked to anomeric carbon atoms of at least two sugar molecules can be prepared with high yield by a method including the step of allowing phenolic hydroxyl groups of a compound having at least two phenolic hydroxyl groups in its molecule to react with sugar molecules each having an acetylated hydroxyl group attached to an anomeric carbon atom in the presence of an organic solvent and an acid catalyst while removing acetic acid formed during the reaction from the reaction system.
Claims4
A method for preparing a glycoside represented by formula (3):
- wherein:
- R1 represents a C1-C10 straight or branched alkyl;
- any one of R2, R3 and R4 represents a hydroxyl;
- each of the remaining two of R2, R3, and R4 represent a residue formed by reacting glucose pentaacetate with a hydroxyl group of an alkyl gallate;
- and
- the method comprises the step of:
- reacting an alkyl gallate having a C1-C10 straight or branched alkyl with glucose pentaacetate in the presence of an organic solvent and an acid catalyst at 30° C. to 60° C. while removing from the reaction system organic solvent and acetic acid formed during the reaction, thereby maintaining the concentration of the acetic acid in the reaction system at 1.0 percent by weight or less during the reaction;
- wherein a distillate comprising said acetic acid and organic solvent both removed from the reaction system is distilled off at a rate of 20 to 500 g/hr relative to one mol of the alkyl gallate having C1-C10 straight or branched alkyl;
- and
- wherein an amount of the substrate concentration is 5 percent to 50 percent by weight.
Dependencies are inferred from the claim text.