Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081561Generated: October 27, 2026

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

https://huagongshe.com/reaction/1081561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantWaterHCID 962—
ReactantRibofuranose, 1-acetate 2,3,5-tribenzoateHCID 10973190—
SolventDichloromethaneHCID 6344—
Product1,3,5-tri-O-benzoyl-alpha-L-ribofuranoseHCID 11048843—

Reaction Conditions

Temperature0 °C

Reaction Steps

Compound 10 (9 g, 17.84 mmol) was stirred in 100 ml of CH2Cl2 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 r.t. for 18 hrs. The organic layer was separated, washed with sat. 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%). m.p. 137°-138° C., lit. 140°-141° C., [α]D =-81.960 (C 0.55, CHCl3 ; D form: [α]D =+83.71.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587362
Source datasetuspto-grants-1996_12
ORD IDord-e471a71760c6441eb848b3d80cf1adb5
Source noteuspto-grants-1996_12