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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358132Generated: October 25, 2026

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

https://huagongshe.com/reaction/358132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantHydrogen iodideHCID 24841—
ReactantDemannoseHCID 161658—
SolventDichloromethaneHCID 6344—
Product2,3:5,6-DI-O-Cyclohexylidene-alpha-D-mannofuranoseHCID 9047407882.6%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of 150 ml of cyclohexanone and 120 ml of dichloromethane were added 10.0 g of D-mannose and 175 mg of hydriodic acid (57%) and the mixture was refluxed with stirring in a water bath at 65° 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 cooling jacket. The reaction mixture was diluted with benzene, washed with aqueous sodium bicarbonate and water and dried over anhydrous magnesium sulfate. The solvent and cyclohexanone were distilled off under reduced pressure to give 11.9 g (82.6%) of 2,3:5,6-di-O-cyclohexylidene-α-D-mannofuranose. After recrystallization from cyclohexane, it melted at 122°-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464530
Source datasetuspto-grants-1984_08
ORD IDord-9298289001374aa3a10a92d9fc57faa9
Source noteuspto-grants-1984_08