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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959581Generated: October 25, 2026

2-Chloropyridine → 3-Chloro-5-(pyridin-2-yloxy)-pyridine

https://huagongshe.com/reaction/1959581

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyridineHCID 7977—
Reactant3-Hydroxy-5-chloropyridineHCID 582305—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product3-Chloro-5-(pyridin-2-yloxy)-pyridineHCID 67077496—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 5-chloro-pyridin-3-ol (1000 mg, 7.72 mmol), potassium tert-butylate (866 mg, 7.72 mmol) and 2-chloro-pyridine (730 g, 7.72 mmol) in DMF (6 mL) was stirred at 130° C. for 3 h. The solvent was removed in vacuo and the residue was partitioned between DCM (50 mL) and 2 N NaOH solution (50 mL). After extraction of the aqueous layer with DCM (6×50 mL) the combined organic layers were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (elution with mixtures of hexane and EA) to give the title compound. MS (m/z): 207.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410134B2
Source datasetuspto-grants-2013_04
ORD IDord-4f8b163bd7784820b517b9b84ba1929d
Source noteuspto-grants-2013_04