HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462591Generated: October 25, 2026
Acetone → 1,2:3,4:5,6-Tris-O-(1-methylethylidene)hexitol
https://huagongshe.com/reaction/1462591
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Mannitol | HCID 6251 | — |
| Product | 1,2:3,4:5,6-Tris-O-(1-methylethylidene)hexitol | HCID 316522 | 96.4% |
Reaction Steps
To 250 ml of acetone were added 10.0 g of D-mannitol and 125 mg of anhydrous cupric chloride, and the mixture was stirred for 8 hours under reflux in a warm-water bath at 58° C. The refluxing solvent was continuously dried with 20 g of molecular sieves 3A which was placed between the reaction vessel and the cooling tube. After the conclusion of the reaction, the acetone was distilled off under reduced pressure, and the residue was dissolved in chloroform. The chloroform solution was washed with aqueous sodium hydrogencarbonate and water, and dried over anhydrous magnesium sulfate. When the chloroform was distilled under reduced pressure, there was obtained 16.0 g (96.4%) of 1,2:3,4:5,6-tri-O-isopropylidene-D-mannitol (purity of not less than 92%). The compound, when recrystallized from 70% ethanol, showed a melting point of 68.5° to 70.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04460767 |
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| Source dataset | uspto-grants-1984_07 |
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| ORD ID | ord-20fa67b0a83847c486c948771b5536f1 |
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| Source note | uspto-grants-1984_07 |
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