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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518258Generated: November 1, 2026

Iodoethane → 5-Bromo-1-ethylpyridin-2(1H)-one

https://huagongshe.com/reaction/518258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178515818HCID 178515818—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-1-ethylpyridin-2(1H)-oneHCID 12210536—

Reaction Steps

To a suspension of NaH (60% dispersion in mineral oil, 1.34 g, 0.056 mol) in THF (10 mL), a solution of 5-bromopyridin-2-ol (2.5 g, 0.014 mol) in THF (50 mL) was added and the resulting mixture was stirred at RT for 1 h. To this mixture, iodoethane (10.9 g, 0.07 mol) was added and the mixture was stirred at RT overnight. The mixture was quenched with water and washed with NH4Cl solution. The organic phase was separated, then concentrated in vacuo and the residue was purified by flash chromatography on silica gel (50-100% PE-AE) to afford 5-bromo-1-ethylpyridin-2(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115141B2
Source datasetuspto-grants-2015_08
ORD IDord-7a5fee37936943a785b9e27f46275b64
Source noteuspto-grants-2015_08