HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856150Generated: October 29, 2026
Glycidyl tosylate, (R)- → HCID 86604801, compound
https://huagongshe.com/reaction/856150
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycidyl tosylate, (R)- | HCID 154187 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178526855 | HCID 178526855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86604801 | HCID 86604801 | 105.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262212B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-075767cda0bd4724be7f8e9bc89f99d5 |
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| Source note | uspto-grants-2007_08 |
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