HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542922Generated: October 26, 2026
Acetone → 1,2:3,4:5,6-Tris-O-(1-methylethylidene)hexitol
https://huagongshe.com/reaction/542922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Mannitol | HCID 6251 | — |
| Reactant | Antimony pentafluoride | HCID 24557 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1,2:3,4:5,6-Tris-O-(1-methylethylidene)hexitol | HCID 316522 | 93.3% |
Reaction Steps
To 200 ml of acetone were added 10.0 g of D-mannitol and 65 mg of antimony pentafluoride, and the mixture was refluxed with stirring in a water bath of 60° C. for 7 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 solution, and the solvent was distilled off under reduced pressure. The residue was dissolved in chloroform, and the solution was washed with aqueous sodium bicarbonate and water, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to give 17.43 g (93.3%) of 1,2:3,4:5,6-tri-O-isopropylidene-D-mannitol. Melting point, 68.5°-70.5° C. (recrystallized from 70% ethanol).
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-a2f9b2ccf0d84d8489e8b26b34173a2b |
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| Source note | uspto-grants-1987_04 |
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