HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → 3,5-Dibromopyridine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 3,5-Dibromo-4-pyridinecarboxaldehyde | HCID 2762998 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 3,5-Dibromopyridine-4-carbonitrile | HCID 42553006 | — |
Reaction Steps
To a solution of 3,5-dibromoisonicotinaldehyde (2.0 g, 0.0075 mol) in formic acid was added hydroxyl amine hydrochloride (14 mL) and concentrated sulfuric acid (5 drops) under argon atmosphere. The reaction mixture was heated to reflux for 8 h. After 8 h, the mixture was cooled to room temperature and concentrated. The residue was dissolved in diethyl ether, washed diethyl ether with saturated solution of sodium bicarbonate, water, saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated to afford the title compound. 1H NMR (400 MHz, CdCl3) δ 8.81 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073929B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-68993533f25b4654882ae8959e1578ee |
| Source note | uspto-grants-2015_07 |