HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-Bromo-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 12542970 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Bromo-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester | HCID 68715975 | 88.2% |
Reaction Steps
To 200 mg (0.67 mmol) of 5-bromo-4-hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester was added 0.5 mL of iodomethane, 200 mg of K2CO3 and 2 mL of DMF. The mixture was stirred at room temperature overnight. The mixture was washed with brine and extracted with ethyl acetate. The combined ethyl acetate layers were washed with brine. Removal of the solvent in vacuo gave 185 mg (88% yield) of 5-bromo-4-methoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07420001B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-c40dd3f64f5d4e6bb18e4e6f9c268dd7 |
| Source note | uspto-grants-2008_09 |