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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017670Generated: October 30, 2026

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

https://huagongshe.com/reaction/1017670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetateHCID 10881213—
SolventTolueneHCID 1140—
Product2-Carboxy-3-(4-fluorophenyl)-furo[3,2-b]pyridineHCID 1106506460.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479507B2
Source datasetuspto-grants-2002_11
ORD IDord-27fdbad67cbd40e7b11382cb25586ec4
Source noteuspto-grants-2002_11