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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225761Generated: November 1, 2026

Iodoethane → 4-Ethyl-3-fluoropyridine

https://huagongshe.com/reaction/225761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantDiisopropylamineHCID 7912—
Reactant3-FluoropyridineHCID 67794—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Ethyl-3-fluoropyridineHCID 1794127035%

Reaction Conditions

Temperature-78 °C

Reaction Steps

nButyllithium (1.6M in tetrahydrofuran, 62.4 ml, 100 mmol) was added dropwise to a solution of diisopropylamine (10 g, 100 mmol) in tetrahydrofuran (110 mL), cooled to −78° C. 3-Fluoropyridine (10 g, 100 mmol) was added dropwise and the reaction mixture was stirred for 1 hour with the temperature maintained below −60° C. Ethyl iodide (31.2 g, 200 mmol) was then added dropwise and the mixture was allowed to stir at room temperature for 30 minutes. The reaction mixture was slowly diluted with water, the solvent was evaporated under reduced pressure and the residue was partitioned between ethyl acetate and water. The organic layer was separated, dried over magnesium sulfate and concentrated in vacuo to give a crude residue. The residue was distilled and title product was obtained during a temperature range of 152-156° C., in 35% yield, 4.46 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557121B2
Source datasetuspto-grants-2009_07
ORD IDord-f33f998aa7554ac8ab263c1d7f1abb1f
Source noteuspto-grants-2009_07