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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358130Generated: October 25, 2026

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

https://huagongshe.com/reaction/358130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPyridineHCID 1049—
ReactantHydrogen iodideHCID 24841—
Reactant(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 3037556—
Product1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranoseHCID 272362959%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 200 ml of acetone were added 10.0 g of D-galactose and 175 mg of hydriodic acid (57%) and the mixture was refluxed with stirring in a water bath at 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 cooling jacket. After completion of the reaction, a small amount of pyridine was added. The acetone was then distilled off under reduced pressure and the residue was dissolved in benzene, washed with aqueous sodium bicarbonate and water and dried over anhydrous magnesium sulfate. The benzene was distilled off and the residue was further distilled under reduced pressure, whereby 8.5 g (59%) of 1,2:3,4-di-O-isopropylidene-α-D-galactopyranose was obtained as a fraction boiling at 129°-133° C./0.2 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464530
Source datasetuspto-grants-1984_08
ORD IDord-e31072d1455645e8abf04f83ad25f564
Source noteuspto-grants-1984_08