HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium borohydride → 2-Bromo-4-nitro-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium borohydride | HCID 169536 | — |
| Reactant | HCID 178526891 | HCID 178526891 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Bromo-4-nitro-1H-imidazole | HCID 47754 | 70,785.398% |
Reaction Steps
Into 1,4-dioxane (1 ml) solution of tetra-n-butylammonium borohydride (638 mg) was added dropwise 1,4-dioxane (1 ml) solution of 2,5-dibromo-4-nitroimidazole (89.5 mg) at a room temperature, after being refluxed the reaction mixture for 23 hours, excessive reagents were quenched by adding concentrated hydrochloric acid, then water and ethyl acetate were added. The organic layer was washed with an aqueous solution being saturated with sodium chloride, then dried over anhydrous sodium sulfate, and purified by a thin layer chromatography (developing agent: ethyl acetate) to obtain 2-bromo-4-nitroimidazole (44.9 g, yield: 71%) of white powdery product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07807843B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-a9fa1162dd004d799e30f1310630ea1e |
| Source note | uspto-grants-2010_10 |