HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydroxy-1-naphthaldehyde → 6-Bromo-2-hydroxy-1-naphthaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydroxy-1-naphthaldehyde | HCID 12819 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-Bromo-2-hydroxy-1-naphthaldehyde | HCID 735457 | 32.9% |
Reaction Steps
To a solution of 2-hydroxy-1-naphthaldehyde (60.0 g) in AcOH (300 mL) was added dropwise a solution of bromine (66.8 g) in AcOH (30 mL) over 30 min. After being stirred for 1 h, the mixture was poured into aqueous Na2S2O3 solution, and the resulting mixture was extracted with AcOEt. The combined organic layers were washed with water, 1N-NaOH, and brine followed by drying over MgSO4. After removal of the solvent in vacuo, the residue was washed with EtOH to give a yellow powder. The powder was crystallized from iPrOH to afford the title compound (28.8 g) as pale yellow needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06649643B1 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-a87524f6e97d4e8f8078701930375b8b |
| Source note | uspto-grants-2003_11 |