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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927258Generated: November 2, 2026

2-Fluoropyridine → (4-(Pyridin-2-yloxymethyl)-phenyl)-methanol

https://huagongshe.com/reaction/1927258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
Reactant1,4-BenzenedimethanolHCID 11506—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product(4-(Pyridin-2-yloxymethyl)-phenyl)-methanolHCID 5925547365.9%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 1,4-benzenedimethanol (5.5 g) and DMF (15 mL) of 2-fluoropyridine (1.3 g) was added NaH (1.4 g/66% in oil) at 0° C., which was stirred for 1 hour at 70° C. The reaction mixture was cooled to room temperature and extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated under a reduced pressure. The residue was purified by NH silica gel column chromatography (ethyl acetate:heptane=1:1) to obtain the titled compound (1.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183264B2
Source datasetuspto-grants-2012_05
ORD IDord-00603c339d724c3f926a814528ded53b
Source noteuspto-grants-2012_05