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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856150Generated: October 29, 2026

Glycidyl tosylate, (R)- → HCID 86604801, compound

https://huagongshe.com/reaction/856150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycidyl tosylate, (R)-HCID 154187—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178526855HCID 178526855—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86604801HCID 86604801105.1%

Reaction Steps

2-Chloro-4-nitro-1H-imidazole (1 g, 6.78 mmol) and (R)-(−)-glycidyl tosylate (1.7 g, 7.45 mmol) were dissolved in tetrahydrofuran (THF) (10 ml), sodium hydrogencarbonate (600 mg, 7.14 mmol) was added to the solution, and the resulting mixture was stirred under reflux for 11 hours. The reaction mixture was concentrated under reduced pressure, water was added to the solution, and the resulting mixture was extracted with ethyl acetate. The organic phase was washed with water and a saturated saline solution in this order, dried over sodium sulfate, and filtered. The filtrate was concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=1/1) to afford (R)-2-chloro-4-nitro-1-(oxiran-2-ylmethyl)imidazole (1.45 g, yield 57%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-075767cda0bd4724be7f8e9bc89f99d5
Source noteuspto-grants-2007_08