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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281667Generated: October 31, 2026

Lithium Hydroxide → 2-Bromo-5,6-dichloro-1-β-D-ribopyranosyl-1H-benzimidazole

https://huagongshe.com/reaction/1281667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantHCID 23383154HCID 23383154—
Solvent1,4-DioxaneHCID 31275—
Product2-Bromo-5,6-dichloro-1-β-D-ribopyranosyl-1H-benzimidazoleHCID 300631775.4%

Reaction Steps

3.0 g (5.7 mmol) 2-Bromo-5,6-dichloro-1-(2,3,4-tri-O-acetyl-beta-D-ribopyranosyl)-1H-benzimidazole was deprotected as outlined in General Procedure V by being dissolved in 60 ml dioxane and the resultant solution cooled in an ice bath between 0 and 5° C. To this solution was added all at once, 22 ml (22 mmol) of 1M aq. LiOH. The mixture was removed from the ice bath and allowed to stir at ambient temperature for 1 h. The mixture was diluted with 120 ml of pH 7 phosphate buffer and extracted with ethyl acetate. The ethyl acetate layer was dried over magnesium sulfate (anhyd.), filtered and solvents evaporated. The residue was triturated in dichloromethane and 1.7 g (4.3 mmol, 75% yield) of 2-bromo-5,6-dichloro-1-beta-D-ribopyranosyl-1H-benzimidazole was collected by vacuum filtration. The product was dried in a vacuum oven at 50° C. overnight; m.p. 175° C. (decomposes): 1H NMR (DMSO-d6) δ7.96 (s,1H), 7.07 (s, 1H), 5.64-5.62 (d, J=9.2 Hz), 5.19-5.17 (d, 1H, J=6.4 Hz), 5.13-5.12 (d, 1H, J=3.2 Hz), 4.86-4.84 (d, 1H, J=6.5 Hz), 4.12-4.06 (m, 1H), 3.98-3.92 (m, 2H), 3.68-3.63 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455507B1
Source datasetuspto-grants-2002_09
ORD IDord-4389c05935c14fd58654bae79098908b
Source noteuspto-grants-2002_09