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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 3037556 | — |
| Product | 1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranose | HCID 2723629 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04464530 |
|---|
| Source dataset | uspto-grants-1984_08 |
|---|
| ORD ID | ord-e31072d1455645e8abf04f83ad25f564 |
|---|
| Source note | uspto-grants-1984_08 |
|---|