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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542916Erstellt: 25. Oktober 2026

Acetone → 1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranose

https://huagongshe.com/reaction/542916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktPyridineHCID 1049—
EduktAntimony pentachlorideHCID 24294—
Edukt(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 3037556—
Produkt1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranoseHCID 272362982,9%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To 200 ml of acetone were added 10.0 g of D-galactose and 89.7 mg of antimony pentachloride, and the mixture was refluxed with stirring in a water bath of 60° C. for 8 hours. During this reaction, the refluxing solvent was dried with 20 g of Molecular Sieves 3A interposed between the reaction vessel and the condenser. After completion of the reaction, a small amount of pyridine was added to the reaction mixture, and the acetone was distilled off under reduced pressure. The residue was dissolved in benzene, and the solution was washed with aqueous sodium bicarbonate and water, and dried over anhydrous magnesium sulfate. The benzene was distilled off, and the resulting residue was distilled under reduced pressure to give 11.97 g (82.9%) of 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose as a fraction having a boiling point of 129°-133° C./0.2 mmHg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04659809
Quelldatensatzuspto-grants-1987_04
ORD IDord-47c4bc940fa54da495d155797d5e485e
Quellennotizuspto-grants-1987_04