HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-Methoxy-2-nitrobenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Hydroxy-2-nitrobenzaldehyde | HCID 39211 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Methoxy-2-nitrobenzaldehyde | HCID 230371 | — |
Reaction Steps
To a suspension of 5-hydroxy-2-nitro-benzaldehyde (10 g, 59.8 mmol) and cesium carbonate (23 g, 70.6 mmol) in DMF (40 mL) was added iodomethane (8.8 mL, 141 mmol), and the mixture stirred at room temperature for 17 h. The resulting red-orange suspension was diluted with ethyl acetate and the mixture was partitioned between ethyl acetate and water. The organic phase was separated and washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated to afford a thick yellow oil which solidified on standing to afford 5-methoxy-2-nitro-benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07442698B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-473f7179d21044e38c07473784bf4a58 |
| Source note | uspto-grants-2008_10 |