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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542918Generated: October 25, 2026

Cyclohexanone → 2,3:5,6-DI-O-Cyclohexylidene-alpha-D-mannofuranose

https://huagongshe.com/reaction/542918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantAntimony pentachlorideHCID 24294—
ReactantDemannoseHCID 161658—
SolventDichloromethaneHCID 6344—
Product2,3:5,6-DI-O-Cyclohexylidene-alpha-D-mannofuranoseHCID 9047407887.3%

Reaction Conditions

Temperature68 °C

Reaction Steps

To a mixed solution consisting of 100 ml of cyclohexanone and 100 ml of dichloromethane were added 10.0 g of D-mannose and 89.7 mg of antimony pentachloride, and the mixture was refluxed with stirring in a water bath of 68° 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. The reaction mixture was diluted with benzene, washed with aqueous sodium bicarbonate and water, and dried over anhydrous magnesium sulfate. The solvents including cyclohexanone were distilled off under reduced pressure to give 16.49 g (87.3%) of 2,3:5,6-di-O-cyclohexylidene-α-D-mannofuranose as a residue. The compound, when recrystallized from cyclohexane, showed m.p. 122°-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659809
Source datasetuspto-grants-1987_04
ORD IDord-86d287f3c21d43de873fa6880be25a48
Source noteuspto-grants-1987_04