HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-Methoxymethyl-2-bromo-4-nitroimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,5-Dibromo-1-methoxymethyl-4-nitroimidazole | HCID 542260 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Methoxymethyl-2-bromo-4-nitroimidazole | HCID 16655131 | 86.9% |
Reaction Steps
Suspension of 2,5-dibromo-1-methoxymethyl-4-nitroimidazole (17.15 g), sodium sulfite (13.73 g), dimethylformamide (100 ml) and water (50 ml) was stirred at a room temperature for 8 hours. The reaction mixture was neutralized with an aqueous solution being saturated with sodium hydrogencarbonate, then ethyl acetate and water were added. The organic layer was washed with an aqueous solution being saturated with sodium chloride, and dried over anhydrous sodium sulfate, then concentrated under a reduced pressure to obtain 2-bromo-1-methoxymethyl-4-nitroimidazole (11.17 g, yield: 86.8%) of white powdery product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368579B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-862729e1b62c45468f4360d89380bf94 |
| Source note | uspto-grants-2008_05 |