HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl (3-(2-hydroxyethyl)benzofuran-7-yloxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | 7-Hydroxy-3-(2-hydroxyethyl)benzofuran | HCID 11159639 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl (3-(2-hydroxyethyl)benzofuran-7-yloxy)acetate | HCID 11230436 | 97% |
Reaction Steps
7-hydroxy-3-(2-hydroxyethyl)benzofuran (1.09 g), methyl bromoacetate (0.86 ml) and potassium carbonate (930 mg) were added to DMF (50 ml) and the mixture was stirred at room temperature for 18 hours. After filtering the reaction solution, the filtrate was concentrated and added to water layer (150 ml), followed by extracting the resultant twice with ethyl acetate (20 ml). After combining the organic layers, the resultant was washed with saturated brine and dried over sodium sulfate. After removing the sodium sulfate by filtration, the solvent was removed under reduced pressure and the residue was purified by column chromatography (solvent: hexane/ethyl acetate=1/1) using silica gel to obtain the desired compound (1.48 g, yield: 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323235B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-d42a97a0e81c45a5a597ed71a8901a06 |
| Source note | uspto-grants-2001_11 |