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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695528Generated: November 1, 2026

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

https://huagongshe.com/reaction/1695528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-Bromobenzyl alcoholHCID 70119—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Product2-((4-Bromobenzyl)oxy)pyridineHCID 24799160—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-fluoropyridine (1.6 g), 4-bromobenzyl alcohol (3.08 g), potassium tert-butoxide (2.03 g) and N-methylpyrrolidone (12.8 ml) was heated at 100° C. by microwave irradiation for one minute. The mixture was diluted with water and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate, filtered and concentrated. 2-(4-Bromobenzyloxy)pyridine was obtained in this way.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163741B2
Source datasetuspto-grants-2012_04
ORD IDord-d90561b0a0bc4163a1862f68761cfb56
Source noteuspto-grants-2012_04