HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542916Generated: October 26, 2026
Acetone → 1,2:3,4-Di-O-isopropylidene-alpha-D-galactopyranose
https://huagongshe.com/reaction/542916
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Antimony pentachloride | HCID 24294 | — |
| 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 | 82.9% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04659809 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-47c4bc940fa54da495d155797d5e485e |
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| Source note | uspto-grants-1987_04 |
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