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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856149Generated: October 29, 2026

Glycidyl tosylate, (R)- → HCID 86604800, compound

https://huagongshe.com/reaction/856149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycidyl tosylate, (R)-HCID 154187—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178526855HCID 178526855—
SolventAcetonitrileHCID 6342—
ProductHCID 86604800HCID 8660480066.3%

Reaction Steps

2-Chloro-4-nitro-1H-imidazole (10 g, 67.79 mmol) and (R)-(−)-glycidyl tosylate (17.02 g, 74.58 mmol) were dissolved in acetonitrile (50 ml), sodium hydrogencarbonate (6.26 g, 74.15 mmol) was added to the solution, and the resulting mixture was stirred under reflux for 3.5 hours. The reaction mixture was allowed to return to room temperature. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=1/2) to afford (R)-2-chloro-1-[2-hydroxy-3-(4-methylbenzenesulfonyloxy)propyl]-4-nitroimidazole (16.9 g, yield 66%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-cc70c9e6cac941f8b1b53043eca39291
Source noteuspto-grants-2007_08