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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429204Generated: October 30, 2026

Ethyl bromoacetate → Ethyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetate

https://huagongshe.com/reaction/429204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-Fluorobenzoyl)-3-hydroxypyridineHCID 22987978—
SolventAcetoneHCID 180—
ProductEthyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetateHCID 10881213102.1%

Reaction Steps

A mixture of give 2-(4-fluorobenzoyl)-3-hydroxypyridine (2.2 g, 11.3 mmol), ethyl bromoacetate (1.6 ml, 14.15 mmol) and potassium carbonate (4.34 g, 31.4 mmol) in acetone (40 ml) was heated at reflux. After 3 h, the reaction was cooled to room temperature, filtered and concentrated in vacuo to give ethyl 2-[2-(4-fluorobenzoyl)pyridin-3-yloxy]acetate (3.5 g) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316464B1
Source datasetuspto-grants-2001_11
ORD IDord-cda20e115c294458aca40971cfc00fe4
Source noteuspto-grants-2001_11