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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715312Generated: October 28, 2026

2-Methyl-5-hydroxypyridine → 2-Bromo-6-methylpyridin-3-ol

https://huagongshe.com/reaction/1715312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantN-bromobutanimideHCID 67184—
SolventPyridineHCID 1049—
Product2-Bromo-6-methylpyridin-3-olHCID 11959101—

Reaction Steps

With cooling with ice, N-bromosuccinimide (18 g) was added to a pyridine (75 ml) solution of 6-methylpyridin-3-ol (10 g), and stirred at room temperature for 4 hours. After further stirred overnight at 50° C., the solvent was evaporated away under reduced pressure. The residue was dissolved in ethyl acetate, and washed with aqueous saturated sodium hydrogencarbonate solution and saturated saline water. After dried, the solvent was evaporated away, and the residue was crystallized with chloroform to obtain the entitled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799820B2
Source datasetuspto-grants-2010_09
ORD IDord-572e83f273fd47dda41bd530fbfef4e5
Source noteuspto-grants-2010_09