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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366073Generated: November 2, 2026

Sodium Hydroxide → HCID 86659956, compound

https://huagongshe.com/reaction/2366073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-(Bromomethyl)pyridine hydrobromideHCID 12707037—
ReactantHCID 178516507HCID 178516507—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 86659956HCID 8665995675%

Reaction Steps

A mixture of 2 g (15.4 mmol) of 2-chloropyridin-4-ol, 3.82 g (15.1 mmol) of 3-(bromomethyl)pyridine hydrobromide, 3 g (75.6 mmol) of sodium hydroxide and 1.39 g (4.3 mmol) of tetrabutylammonium bromide in 90 mL of toluene is refluxed for 12 hours. After cooling to room temperature, the reaction medium is taken up in 300 mL of EtOAc, washed successively with water (2×100 mL), with saturated NaHCO3 solution (100 mL) and with brine (100 mL), dried over Na2SO4, filtered, concentrated under reduced pressure and then purified by chromatography on silica gel, eluting with a 98/2 DCM/MeOH mixture. 2.5 g of 2-chloro-4-(pyridin-3-ylmethoxy)pyridine are obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697731B2
Source datasetuspto-grants-2014_04
ORD IDord-5e9b8b64325943bbb91386e2650e481c
Source noteuspto-grants-2014_04