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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526071Generated: October 30, 2026

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

https://huagongshe.com/reaction/1526071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSulfuric AcidHCID 1118—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(5-Bromopyridin-3-yl)acetic acidHCID 2802539—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(5-bromopyridin-3-yl)acetateHCID 54116619—

Reaction Steps

1.00 g (4.63 mmol) (5-bromopyridin-3-yl)acetic acid are initially introduced into 20 ml ethanol, 2 ml conc. sulfuric acid are added and the mixture is stirred under reflux overnight. The reaction solution is introduced on to a mixture of 100 ml saturated sodium bicarbonate solution and 100 ml ethyl acetate, while stirring, and the aqueous phase is extracted with ethyl acetate (three times with 50 ml each time). The combined organic phases are dried over sodium sulfate, filtered and concentrated and the residue is freed from solvent residues overnight in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085572B2
Source datasetuspto-grants-2015_07
ORD IDord-f7575e09517446b58a8ebfd7e939b2fc
Source noteuspto-grants-2015_07