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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358131Generated: October 27, 2026

Acetone → 2,3:5,6-Di-O-isopropylidene-alpha-D-mannofuranose

https://huagongshe.com/reaction/358131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPyridineHCID 1049—
ReactantHydrogen iodideHCID 24841—
ReactantDemannoseHCID 161658—
Product2,3:5,6-Di-O-isopropylidene-alpha-D-mannofuranoseHCID 715718880%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 200 ml of acetone were added 10.0 g of D-mannose and 100 mg of hydrogen iodide and the mixture was refluxed with stirring in a water bath at 60° C.for 5 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 under reduced pressure to give 11.5 g (80%) of 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose. After recrystallization from petroleum ether, it melted at 122°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464530
Source datasetuspto-grants-1984_08
ORD IDord-291c44cfc18946fcb3ccda5d5e62eb6d
Source noteuspto-grants-1984_08