Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37893Generated: October 26, 2026

Ethanol → Ethyl 2-(5-bromopyridin-3-yl)acetate

https://huagongshe.com/reaction/37893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-(5-Bromopyridin-3-yl)acetic acidHCID 2802539—
CatalystSulfuric AcidHCID 1118—
ProductEthyl 2-(5-bromopyridin-3-yl)acetateHCID 54116619—

Reaction Steps

5.0 g (23.1 mmol) of (5-bromopyridin-3-yl)acetic acid in 30 ml of ethanol and 25 drops of conc. sulfuric acid are stirred at boiling point for 16 h. For work-up, the reaction mixture is concentrated under reduced pressure, the residue is taken up in ethyl acetate and washed repeatedly with semiconcentrated sodium bicarbonate solution, the organic phase is dried over sodium sulfate, the drying agent is filtered off, the solvent is removed completely on a rotary evaporator and the product is dried under reduced pressure for 16 h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524699B2
Source datasetuspto-grants-2013_09
ORD IDord-e24430d98d0a4aaf9fb307533163ce10
Source noteuspto-grants-2013_09