HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Bromo-2,5-dimethoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-2-hydroxy-5-methoxybenzaldehyde | HCID 735818 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Bromo-2,5-dimethoxybenzaldehyde | HCID 931096 | 67% |
Reaction Steps
A solution of 50 (10 g, 43 mmol), Methyl Iodide (7.3 g, 52 mmol), and K2CO3 (12 g, 86 mmol) in acetone (200 ml) was heated to reflux. After 4 hr, the reaction was cooled, poured into water and extracted with ether. The ether layer was dried concentrated and the product was purified by silica gel column chromatography (10%EtOAc/Hex) to give 51 as a solid (7.0 g, 67%): Mp=62-64° C.; 1H NMR (CDCl3) δ 10.32 (s, 1 H), 7.38 (d, 1 H, J=2.8 Hz), 7.28 (d, 1 H, J=3.2 Hz), 3.93 (s, 3 H), 3.82 (s, 3 H); MS 245/247 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06774248B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-c6efdafc0e6a46ea957d4f6078fca6f8 |
| Source note | uspto-grants-2004_08 |