HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-5-hydroxybenzaldehyde → HCID 72313051, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-5-hydroxybenzaldehyde | HCID 387179 | — |
| Reactant | O-tert-butylhydroxylamine hydrochloride | HCID 2777906 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 72313051 | HCID 72313051 | 66.1% |
Reaction Steps
To the solution of 2-bromo-5-hydroxy-benzaldehyde (402 mg, 2 mmol) in methanol (10 ml) is added O-tert-butyl-hydroxylamine hydrochloride (125 mg, 10 mmol). The mixture is stirred at room temperature overnight. The resulting mixture is diluted with ethyl acetate, washed with brine, dried over MgSO4, and evaporated to afford the titled compound (360 mg) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609892B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-2f760ec5aebf4cc5aba411e41227184e |
| Source note | uspto-grants-2013_12 |