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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712636Generated: October 31, 2026

Methyl iodide → 3-Bromo-4-(methoxymethyl)pyridine

https://huagongshe.com/reaction/712636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(3-Bromopyridin-4-yl)methanolHCID 46840038—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-4-(methoxymethyl)pyridineHCID 6671405084.8%

Reaction Steps

To a solution of (3-bromo-pyridin-4-yl)-methanol (300 mg, 1.6 mmol) in THF (50 mL) at 0° C. is added 60% NaH (96 mg, 2.4 mmol). Then the mixture is stirred at room temperature for 30 min. MeI (270 mg, 1.9 mmol) is added to the mixture at 0° C. and again the mixture is stirred at room temperature for 4 hrs. Then the reaction is quenched with saturated NH4Cl aqueous solution and the mixture is extracted with EtOAc. The organic layer is separated, dried and concentrated to give the crude product. Purification by prep-TLC affords 274 mg of 3-bromo-4-methoxymethyl-pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-a6443b9e53f24762bc23e1c1fa59505e
Source noteuspto-grants-2015_11