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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691003Generated: October 26, 2026

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

https://huagongshe.com/reaction/1691003

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 numberUS08153662B2
Source datasetuspto-grants-2012_04
ORD IDord-ccbe8ed238f54e04a46fbd32d98f5545
Source noteuspto-grants-2012_04