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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787414Generated: October 27, 2026

Hydrogen Bromide → 1,3,5-tri-O-benzoyl-alpha-L-ribofuranose

https://huagongshe.com/reaction/1787414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantDichloromethaneHCID 6344—
ReactantRibofuranose, 1-acetate 2,3,5-tribenzoateHCID 10973190—
SolventWaterHCID 962—
Product1,3,5-tri-O-benzoyl-alpha-L-ribofuranoseHCID 11048843150.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Compound 10 (9 g, 17.84 mmol) was stirred in 100 mL of CH2C12 at 0° C. while 70 mL of CH2Cl2 containing HBr (3.2 g, 30.5 mmol) was added in one portion. The mixture was stirred at 0° C. for 3.5 hrs, water (55 ml) was added and the mixture stirred at room temperature for 18 hours. The organic layer was separated, washed with saturated NaHCO3, dried (MgSO4). After evaporation of the solvent, a foam was obtained, which upon recrystallization from CH2Cl2 and n-hexane, gave 11 as a white solid (6.2 g, 75.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511027B2
Source datasetuspto-grants-2009_03
ORD IDord-fdaeae1224e84dbf81af983a18131230
Source noteuspto-grants-2009_03