HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl (5-bromobenzofuran)-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-Bromo-2-benzofurancarboxylic acid | HCID 735247 | — |
| Product | Ethyl (5-bromobenzofuran)-2-carboxylate | HCID 735184 | 93% |
Reaction Steps
A solution of 5-bromo-2-benzofurancarboxylic acid (5.01 g, 20.8 mmol) in absolute ethanol (150 ml) was added with concentrated sulfuric acid (15 ml) and the mixture was refluxed under stirring for 2 h. After this time, the volatiles were evaporated off under reduced pressure and the resulting residue was neutralized with a sodium bicarbonate saturated solution and extracted with ethyl ether (4×100 ml). The mixture was dried and the solvent was evaporated off under reduced pressure, to obtain 5.19 g of the title compound as a white solid with melting point 58-60° C. (93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05990142 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-bb9ab76924f3425d8d8322bc3fee41ba |
| Source note | uspto-grants-1999_11 |