HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-Bromo-3-nitro-2-pyridinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,6-Dibromo-3-nitropyridine | HCID 555053 | — |
| Reactant | Ethanol, reaction products with ammonia, distn. residues | HCID 22020343 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Bromo-3-nitro-2-pyridinamine | HCID 12097745 | — |
Reaction Steps
To a suspension of 2,6-dibromo-3-nitropyridine (5.00 g) in ethanol (10 ml) was added an ammonia/ethanol solution (6.8 M, 15 ml) at room temperature, and the mixture was placed in a closed reaction vessel and stirred at room temperature for 19 hr. To the reaction mixture was added water (25 ml), and the precipitate was collected by filtration. The precipitate was washed with ethanol, suspended in ethanol (55 ml), heated and cooled. The precipitate was collected by filtration to give the objective compound (3.19 g) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06911469B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-ce7b1a9e7b1f4f2498cc96818a00a82d |
| Source note | uspto-grants-2005_06 |