HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 6-Bromo-5-methoxypicolinaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Persulfate | HCID 24412 | — |
| Reactant | 2-Bromo-3-methoxy-6-methylpyridine | HCID 10965563 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | 6-Bromo-5-methoxypicolinaldehyde | HCID 22268339 | 24% |
Reaction Steps
A stirred mixture of 2-bromo-3-methoxy-6-methyl-pyridine (2.00 g, 9.9 mmol), Cu(II) sulfate pentahydrate (2.47 g, 9.9 mmol), and potassium peroxydisulfate (8.03 g, 29.7 mmol) in 80 mL of acetonitrile/H2O (1:1) was heated under reflux. After 1 hour, the dark green mixture was cooled to room temperature and CH2Cl2 was added. The layers were separated and the aqueous layer further extracted with CH2Cl2. The organics were combined, dried (MgSO4), filtered and evaporated. The resulting crude product was purified on silica gel [Biotage, hexane:ethyl acetate (4:1)] to give a white solid (0.51 g, 24% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06515003B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-833df49558c141e0a2b203b940cc3eb3 |
| Source note | uspto-grants-2003_02 |