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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340472Generated: October 29, 2026

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

https://huagongshe.com/reaction/340472

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 numberUS08895585B2
Source datasetuspto-grants-2014_11
ORD IDord-eed2cc3d6dfb422cbb630b89fb5ffbf3
Source noteuspto-grants-2014_11