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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850118Generated: October 29, 2026

Diethyl Ether → 5-Bromo-2-ethylpyridine

https://huagongshe.com/reaction/850118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant2,5-DibromopyridineHCID 69353—
ReactantHCID 178418443HCID 178418443—
CatalystZincchlorideHCID 3007855—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-ethylpyridineHCID 1397973676%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethylmagnesium bromide in ether (100 ml, 3M, 0.3 mol) was added dropwise to a cold (5° C.) solution of anhydrous zinc chloride (40.9 g, 0.3 mol) in THF (500 ml) under nitrogen. After stirring for one hour at 0° C., tetrakis(triphenylphosphine)-palladium (0) (1.0 g, 0.87 mmol) was added followed by a solution of 2,5-dibromopyridine (50 g, 0.21 mol) in THF (200 ml). The resulting yellow suspension was stirred at room temperature overnight, quenched by the addition of water (200 ml) and then evaporated in vacuo. The residue was treated with a suspension of ethylenediaminetetraacetic acid (200 g) in water (1000 ml) and dichloromethane (500 ml). The organic layer was separated and the aqueous layer again extracted with dichloromethane (500 ml). The combined extracts were dried (MgSO4), solvent evaporated in vacuo, and the residue distilled (123-124° C., 60 mmHg) to give the required product as a colourless oil (28.8 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06015825
Source datasetuspto-grants-2000_01
ORD IDord-6066826c41484cc78574173cd1051802
Source noteuspto-grants-2000_01