HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → Ethyl 5-bromo-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromobenzo[b]furan-3(2H)-one | HCID 10512748 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 5-bromo-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylate | HCID 58458886 | — |
Reaction Steps
Potassium carbonate (1.66 g, 12 mmol) is added to a solution of 5-bromo-1-benzofuran-3(2H)-one (2.13 g, 10 mmol) in acetone (25 mL). The stirred mixture is treated dropwise with ethyl chloroformate (1.05 mL, 11 mmol). The mixture is then heated at reflux for 18 h. The solids are filtered off and the filtrate concentrated in vacuo. The residue is partitioned between EtOAc and saturated aqueous NaHCO3. The layers are separated and the organic layer washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by silica gel chromatography (gradient elution with hexanes-EtOAc) to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296750B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-591bf07ed2904349b7415ea6bc6a6304 |
| Source note | uspto-grants-2016_03 |