HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846996Generated: November 2, 2026
Sodium Iodide → 1-(3,3-Dimethoxypropyl)-7-methoxyquinoxalin-2(1H)-one
https://huagongshe.com/reaction/1846996
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | 3-Bromopropionaldehyde dimethylacetal | HCID 118932 | — |
| Reactant | 7-Methoxy-1,2-dihydroquinoxalin-2-one | HCID 491319 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(3,3-Dimethoxypropyl)-7-methoxyquinoxalin-2(1H)-one | HCID 86724927 | 72% |
Reaction Steps
7-Methoxyquinoxalin-2(1H)-one (synthesized with reference to WO2009/1126; 4.13 g, 23.4 mmol) was dissolved in N,N-dimethylformamide (103 ml). The solution was cooled in an ice bath, lithium hydride (purity 90%, 248 mg, 28.1 mmol) was then added thereto and the mixture was stirred at room temperature for 40 minutes. The reaction solution was cooled in an ice bath again, 3-bromo-1,1-dimethoxypropane (3.78 ml, 28.1 mmol) and sodium iodide (4.21 g, 28.1 mmol) were added and then the mixture was stirred at room temperature for 2 days. The reaction solution was diluted with ethyl acetate, washed sequentially with saturated sodium chloride solution (×2), water and saturated sodium chloride solution, dried over magnesium sulfate and the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to yield 4.68 g (72%) of the title compound in the form of a yellow syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08952010B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-9ad34cbd113e4d54b35af0aa459d6b5f |
|---|
| Source note | uspto-grants-2015_02 |
|---|