Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963232Generated: October 29, 2026

Dimethylformamide → 2-Bromo-5-chloro-3-methoxypyridine

https://huagongshe.com/reaction/963232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-5-chloropyridin-3-olHCID 14740053—
SolventWaterHCID 962—
Product2-Bromo-5-chloro-3-methoxypyridineHCID 19081434—

Reaction Steps

To a DMF (60 mL) solution containing 2-bromo-5-chloro-3-hydroxypyridine (19.95 g, 95.7 mmol) at 0° C. was added NaH (2.53 g, 105.3 mmol) portion wise. After the cessation of H2 evolution, CH3I (14.26 g, 100.5 mmol) was added dropwise and the reaction stirred ~16 h. Water (1.9 mL) was added and the solvent removed under reduced pressure. The concentrate was triturated with 5 portions of CH2Cl2. The combined organic phases were washed with sat. NaCl solution, dried with K2CO3, filtered, and concentrated in vacuo. Silica gel chromatography (95:5 Hexane:EtOAc) of the concentrate afforded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763444
Source datasetuspto-grants-1998_06
ORD IDord-02d974ba0a9744c0992196be9d522c6f
Source noteuspto-grants-1998_06