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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620079Generated: October 31, 2026

Dimethylformamide → 3-Bromo-5-(methoxymethyl)pyridine

https://huagongshe.com/reaction/1620079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(5-Bromo-3-pyridinyl)methanolHCID 2784733—
SolventWaterHCID 962—
Product3-Bromo-5-(methoxymethyl)pyridineHCID 18624569—

Reaction Steps

Sodium hydride (61% in oil) (11 mg) was added to a DMF (0.9 ml) solution containing (5-bromopyridin-3-yl)methanol (34 mg) under ice cooling, followed by stirring for 1 hour. Then, methyl iodide (17 μl) was added, followed by stirring at room temperature for 13 hours. Thereafter, water was added to the reaction solution, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Subsequently, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=4:1 to 1:1), and a light yellow solid of 3-bromo-5-(methoxymethyl)pyridine (26.5 mg) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772320B2
Source datasetuspto-grants-2014_07
ORD IDord-c1fc2a3de1464bd99069b210e4f32e05
Source noteuspto-grants-2014_07