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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691387Generated: November 1, 2026

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

https://huagongshe.com/reaction/1691387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-FluoropyridineHCID 9746—
Reactant4-Bromobenzyl alcoholHCID 70119—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-((4-Bromobenzyl)oxy)pyridineHCID 2479916099%

Reaction Conditions

Temperature54 °C

Reaction Steps

To a solution of 4-bromobenzyl alcohol (25 g, 130 mmol) in N,N-dimethyl formamide (125 mL) was added potassium tert-butoxide (15.8 g, 141 mmol) at room temperature, which was stirred at 54° C. for 10 minutes. To this reaction solution was added 2-fluoropyridine (15 mL, 154 mmol) at from 40° C. to 58° C., which was further stirred for 30 minutes at 65° C. The reaction solution was allowed to room temperature, water and ethyl acetate were added, and liquid separation was carried out. The aqueous layer was further extracted with ethyl acetate (twice). The ethyl acetate layers were combined, washed with water (3 times) and sodium chloride water (once), dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under a reduced pressure. Diethyl ether was added to the residue, which was concentrated under a reduced pressure to obtain the title compound (34 g) as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-e168f596280f46dabaca2e4959c6cd76
Source noteuspto-grants-2012_04