Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782010Generated: October 29, 2026

Diethyl Ether → Ethyl (6-bromo-2-nitropyridin-3-yloxy)acetate

https://huagongshe.com/reaction/1782010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromo-2-nitropyridin-3-olHCID 21873808—
CatalystEthyl bromoacetateHCID 7748—
SolventAcetoneHCID 180—
ProductEthyl (6-bromo-2-nitropyridin-3-yloxy)acetateHCID 5956064989%

Reaction Steps

The hydroxypyridine (f) (30 g, 0.14 mol) was suspended in acetone (200 ml), and potassium carbonate (39 g, 0.28 mol) was added, followed by ethyl bromoacetate (15.7 ml, 0.14 mmol). The reaction was heated at reflux for 10 hours, then was cooled to room temperature and diluted with Et2O. The precipitate was removed by suction filtration, and the filtrate was concentrated in vacuo to afford material (38 g, 89%), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498326B2
Source datasetuspto-grants-2009_03
ORD IDord-1771243a14b444e290dbf8af8b46e80b
Source noteuspto-grants-2009_03