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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406765Generated: October 30, 2026

Ethyl bromoacetate → ethyl 2-(5-bromo-2-oxopyridin-1(2H)-yl)acetate

https://huagongshe.com/reaction/406765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-hydroxypyridineHCID 599528—
SolventDimethylformamideHCID 6228—
Productethyl 2-(5-bromo-2-oxopyridin-1(2H)-yl)acetateHCID 2883426157.7%

Reaction Steps

To a solution of compound 5-bromopyridin-2(1H)-one (348 mg, 2.0 mmol) and K2CO3 (830 mg, 6.0 mmol) in DMF (15 mL) was added ethyl bromoacetate dropwise. The mixture was stirred at room temperature for 2 h, filtered, and the filtrate was concentrated in vacuo. The residue was purified by prep TLC (1:1 PE/EtOAc) to afford ethyl 2-(5-bromo-2-oxopyridin-1(2H)-yl)acetate (300 mg, 57.7%). 1H NMR CDCl3: δ 7.41-7.26 (m, 2H), 6.53-6.5 (d, 1H), 4.59 (s, 2H), 4.28-4.21 (q, 2H), 1.32-1.23 (q, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754076B2
Source datasetuspto-grants-2014_06
ORD IDord-df39723091c4459a84e40c31bf191731
Source noteuspto-grants-2014_06