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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358127Generated: October 25, 2026

Acetone → 2,3-O-Isopropylidene-D-ribofuranose

https://huagongshe.com/reaction/358127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantHydrogen iodideHCID 24841—
ReactantSodium BicarbonateHCID 516892—
ReactantAldehydo-D-riboseHCID 5311110—
Product2,3-O-Isopropylidene-D-ribofuranoseHCID 1100871230%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 200 ml of acetone were added 10.0 g of D-ribose and 175 mg of hydriodic acid (57%) and the mixture was refluxed with stirring in a water bath at 60° C. for 6 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 aqueous sodium bicarbonate 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 sodium sulfate. The benzene was distilled off under reduced pressure and the residue was further distilled under reduced pressure, whereby 3.84 g (30%) of 2,3-O-isopropylidene-D-ribofuranose was obtained as a fraction boiling at 108°-111° C./0.04 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464530
Source datasetuspto-grants-1984_08
ORD IDord-47de20d62a9947a8bef92903a162a5f0
Source noteuspto-grants-1984_08