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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77896Generated: October 23, 2026

Dimethylformamide → 2-(4-Bromo-benzyloxy)4-methyl-pyridine

https://huagongshe.com/en/reaction/77896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromobenzyl alcoholHCID 70119—
Reactant2-Fluoro-4-methylpyridineHCID 2737403—
SolventWaterHCID 962—
Product2-(4-Bromo-benzyloxy)4-methyl-pyridineHCID 5925528858.8%

Reaction Steps

To a mixture of 4-bromobenzyl alcohol (4.54 g, 24.3 mmol) and N,N-dimethylformamide (50.0 mL) were added sodium hydride (1.00 g, 25.0 mmol, 60% in oil) was added at 0° C. under nitrogen atmosphere, which was stirred for 50 minutes at room temperature. 2-Fluoro-4-methylpyridine (1.80 g, 16.2 mmol) was then added thereto at 0° C., and stirred for 2 hours and 30 minutes at room temperature. Water was added to the reaction solution at room temperature, which was then extracted with ethyl acetate. The organic layer was separated, washed with saturated aqueous sodium chloride, and filtered. The filtrate was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:heptane=1:15) to obtain the title compound (2.65 g, 58.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-79efb6ff36ff47b189d35a939edd6e29
Source noteuspto-grants-2014_09