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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170034Generated: October 31, 2026

Methyl iodide → 5-bromo-2-(methoxymethyl)Pyridine

https://huagongshe.com/reaction/2170034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(5-Bromopyridin-2-yl)methanolHCID 5200169—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product5-bromo-2-(methoxymethyl)PyridineHCID 54044357102.6%

Reaction Steps

A solution of this (5-bromo-pyridin-2-yl)-methanol (4.80 g, 23.0 mmol) in DMF (25 mL) was added drop wise over 5 minutes to a slurry of sodium hydride (1.10 g, 27.8 mmol) in DMF (50 mL) at 0° C. under N3. The mixture was stirred for 15 minutes before the drop wise addition of a solution of methyl iodide (1.57 mL, 25.3 mmol) in DMF (25 mL). The mixture was allowed to reach room temperature and was then stirred overnight. The mixture was poured into brine and extracted with EtOAc. The combined organic layers were thoroughly washed with brine, dried over MgSO4 and evaporated to dryness to give the title compound as a yellow oil (4.77 g, 98%) sufficiently pure for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050327B2
Source datasetuspto-grants-2015_06
ORD IDord-3c4f4d40391545909f27dd21eef5618c
Source noteuspto-grants-2015_06