HuagongsheHuagongshe Chemistry Print Report · For research reference only
Salicylaldehyde → Ethyl 1-benzofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 1-benzofuran-2-carboxylate | HCID 641368 | 33.1% |
Reaction Steps
A mixture of salicylaldehyde (53.10 g), K2CO3 (97 g) and ethyl bromoacetate (73.30 g) in ethanol (200 ml) was refluxed for 6 hours. The reaction mixture was diluted with ethyl acetate, washed with water, 1N NaOH and brine, dried and concentrated to give the titled compound (27.40 g) as a colorless oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420375B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-ae38583c3e414d89be098a3b3bb75a61 |
| Source note | uspto-grants-2002_07 |