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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960085Generated: October 29, 2026

2-Fluoropyridine → 2-((4-Bromobenzyl)oxy)pyridine

https://huagongshe.com/reaction/1960085

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
Reactant4-Bromobenzyl alcoholHCID 70119—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantSodium chloride; waterHCID 57417360—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product2-((4-Bromobenzyl)oxy)pyridineHCID 2479916097.6%

Reaction Steps

To a solution of 4-bromobenzyl alcohol (18 g, 94.3 mmol) in dimethylsulfoxide (85 mL) was added potassium tert-butoxide (11.5 g, 99 mmol) little by little under a nitrogen atmosphere at room temperature, which was stirred for 10 minutes. To this solution was added 2-fluoropyridine (12.3 g, 123 mmol) dropwise over 30 minutes under a water bath cooling. After stirring at room temperature for two hours, ethyl acetate and 5% sodium chloride water were added, and extracted. After the organic layer was washed sequentially with water and 5% sodium chloride water, the solvent was evaporated under a reduced pressure, so as to obtain the title compound (24.3 g) as a yellow oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410277B2
Source datasetuspto-grants-2013_04
ORD IDord-e14090f0160c4d018829c2b299a4f264
Source noteuspto-grants-2013_04