HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 54497110, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 18779202 | HCID 18779202 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54497110 | HCID 54497110 | — |
Reaction Steps
A solution of the aldehyde from step A (0.13 g, 0.61 mmol), methoxylamine hydrochloride (61 mg, 0.735 mmol) and pyridine (2 mL) in EtOH (10 mL) was heated at reflux for 16 h. Further portions of methoxylamine hydrochloride (61 mg, 0.735 mmol) and pyridine (2 mL) were added and heating was continued for 24 h. The solution was cooled, diluted with EtOAc, extracted with water (2×) then brine, dried and concentrated to give the title compound as an oil. This was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06080870 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-2d22cb29773c4e2ea8f084b6d124b626 |
| Source note | uspto-grants-2000_06 |