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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437331Generated: October 29, 2026

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

https://huagongshe.com/reaction/1437331

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 mole) was suspended in acetone (200 mL), and potassium carbonate (39 g, 0.28 mole) was added, followed by ethyl bromoacetate (15.7 mL, 0.14 mmole). The reaction was heated at reflux for 10 hr, 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 numberUS07622481B2
Source datasetuspto-grants-2009_11
ORD IDord-9c83eb389e8a4f368b5ca90765417f68
Source noteuspto-grants-2009_11