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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429205Generated: October 29, 2026

2-Carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridine → 3-(4-Fluorophenyl)-furo[3,2-b]pyridine

https://huagongshe.com/reaction/429205

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridineHCID 11065064—
CatalystCopperHCID 23978—
SolventQuinolineHCID 7047—
Product3-(4-Fluorophenyl)-furo[3,2-b]pyridineHCID 2298798557%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316464B1
Source datasetuspto-grants-2001_11
ORD IDord-d8b88c8b0ffc4fe2979cce21aecaf622
Source noteuspto-grants-2001_11