Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930751Generated: October 29, 2026

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

https://huagongshe.com/reaction/1930751

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-dimethylformamide (125 mL) was added potassium tert-butoxid at room temperature, which was stirred for 10 minutes at 54° C. To this reaction solution was added 2-fluoropyridine (15 mL, 154 mmol) at a temperature of from 40° C. to 58° C., which was stirred for another 30 minutes at 65° C. The reaction solution was cooled to room temperature, water and ethyl acetate were added to separate the reaction solution. The aqueous layer was further extracted (twice) with ethyl acetate. This was combined with an ethyl acetate layer, washed with water (three times) and saline (once), and was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under a reduced pressure. Diethyl ether was added to the residue, and this was concentrated under a reduced pressure, so as to obtain a crude product of the titled compound (34 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188119B2
Source datasetuspto-grants-2012_05
ORD IDord-ec9be5a30e994da99f383400a3633ded
Source noteuspto-grants-2012_05