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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474306Generated: November 1, 2026

Sodium Hydroxide → 5-Bromo-2-chloro-4-methoxypyridine

https://huagongshe.com/reaction/1474306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Chloro-4-methoxypyridineHCID 1991128—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product5-Bromo-2-chloro-4-methoxypyridineHCID 49853415—

Reaction Steps

To a solution of 2-chloro-4-methoxypyridine (10.0 g, 69.7 mmol) in 50 mL of sulfuric acid at 0° C. was added NBS. The reaction mixture was allowed to stir and warm up to room temperature for 2 hour and then heated at 60° C. for 5 h. Then it was cooled to room temperature and neutralized with 1 N NaOH (pH˜7), diluted with water (50 mL) and the aqueous layer was extracted with ethyl acetate (2×100 mL). The organic layers were washed with water (2×50 mL), sat. NaHCO3, brine, dried over Mg2SO4 and concentrated to provide an oil, which was chromatographed. On elution with 0-25% EtOAc/hexanes, of the final product was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-1001686050274d31b97f6e61dbb9cd19
Source noteuspto-grants-2015_04