HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridine → 3-(4-Fluorophenyl)-furo[3,2-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridine | HCID 11065064 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Quinoline | HCID 7047 | — |
| Product | 3-(4-Fluorophenyl)-furo[3,2-b]pyridine | HCID 22987985 | 57% |
Reaction Steps
A mixture of 2-carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridine (1.8 g, 7 mmol), copper metal (0.56 g, 8.81 mmol) in quinoline (10 ml) was heated at reflux. After 45 min., the reaction was cooled to room temperature and the product was extracted into water. The aqueous layer was acidified with hydrochloric acid and acetic acid. The product was filtered and dissolved in ether. The ether layer was dried over sodium sulfate and concentrated in vacua. Purification by flash chromatography using ethyl acetate-hexanes (1:9) as the eluant gave 3-(4-fluorophenyl)-furo[3,2-b]pyridine as a solid (0.85 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06316464B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-d8b88c8b0ffc4fe2979cce21aecaf622 |
| Source note | uspto-grants-2001_11 |