HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-Bromo-5-nitro-thiophene-2-carbaldehyde oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 4-Bromo-5-nitrothiophene-2-carbaldehyde | HCID 21886281 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Bromo-5-nitro-thiophene-2-carbaldehyde oxime | HCID 73852152 | 88% |
Reaction Steps
Hydroxylamine hydrochloride (85 g, 1.2 mol) was added to a solution of 4-bromo-5-nitro-thiophene-2-carbaldehyde (234 mg, 0.529 mmol, Example 286: step a) in EtOH (7.5 mL, 200 proof—anhydrous):pyridine (100 mL, anhydrous) at rt over 5 min. The reaction mixture was heated to reflux overnight, then cooled to rt. The solvents were removed in vacuo resulting in a solid residue that was washed with water and filtered. The solid was dried overnight under high vacuum to afford the title compound as a yellow solid (225 g, 88%). The solid was used for the next step without further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138530B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-43f2ba13baec47cf9648112fe3674629 |
| Source note | uspto-grants-2006_11 |