HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycidyl tosylate, (R)- → HCID 86604800, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycidyl tosylate, (R)- | HCID 154187 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178526855 | HCID 178526855 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86604800 | HCID 86604800 | 66.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07262212B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-cc70c9e6cac941f8b1b53043eca39291 |
| Source note | uspto-grants-2007_08 |