HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → 2-Carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetate | HCID 10881213 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridine | HCID 11065064 | 60.9% |
Reaction Steps
Sodium ethoxide (1.51 g. 22.6 mmol) was suspended in toluene (25 ml) and ethyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetate (3.5 g, 11.5 mmol) was added. The reaction was heated at reflux under an argon atmosphere. After 12 h, the reaction mixture was cooled to room temperature and the product was extracted into water. The aqueous layer was acidified with hydrochloric acid to give 2-carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridine as a solid (1.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06630485B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-f6a8a60873a748c0905b1373ceb9ef1b |
| Source note | uspto-grants-2003_10 |